K183393 · Joytech Healthcare Co. , Ltd. · FLL · Nov 18, 2019 · General Hospital
Device Facts
Record ID
K183393
Device Name
Digital Thermometer
Applicant
Joytech Healthcare Co. , Ltd.
Product Code
FLL · General Hospital
Decision Date
Nov 18, 2019
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 880.2910
Device Class
Class 2
Attributes
Pediatric
Indications for Use
The Digital Thermometers DMT series(Except DMT-455) are intended to measure the human body temperature in regular mode orally, rectally or under the arm. And the devices are reusable for clinical or home use on people of all ages, including children under 8 with adult supervision. The device model DMT-455 is intended to measure temperature orally, and the device is reusable for clinical or home use for children less than 4 years old with adult supervision.
Device Story
Digital thermometers measure human body temperature via thermistor sensor; resistance changes with temperature; integrated circuit (IC) converts resistance to frequency; MCU calculates temperature; result displayed on LCD. Reusable devices for clinical/home use; operated by patients or clinicians. Models vary by tip type (flexible/rigid), response time, and features (backlight, predictive mode). Output informs clinical decision-making regarding fever management. Patient-contacting materials include stainless steel, TPE, and ABS.
Clinical Evidence
Clinical testing conducted on models DMT-4726 and DMT-4735 per ISO 80601-2-56. Study included 450 subjects across three age groups: infants (newborn to 1 year), children (>1 to 5 years), and adults (>5 years). Results demonstrated compliance with ISO 80601-2-56 requirements.
Technological Characteristics
Materials: Stainless steel, TPE, ABS. Sensing: Thermistor-based resistance change. Energy: 1.5V button battery (LR41/SR41) or 3.0V CR2032. Connectivity: None. Sterilization: Not specified. Standards: ISO 80601-2-56:2017, ASTM E1112, IEC 60601-1, IEC 60601-1-2, ISO 10993-5/10.
Indications for Use
Indicated for human body temperature measurement (oral, rectal, or axillary) in clinical or home settings for all ages. DMT-455 indicated for oral use only in children <4 years. All use requires adult supervision for children.
Regulatory Classification
Identification
A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover.
Special Controls
(1) Device is not a clinical thermometer with telethermographic functions;
(2) Device is not a clinical thermometer with continuous temperature measurement functions; and
(3) Appropriate analysis and testing (such as that outlined in the currently FDA-recognized editions, as appropriate, of ISO 80601-2-56, “Medical electrical equipment—Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement,” or ASTM E1965, “Standard Specification for Infrared Thermometers for Intermittent Determination of Patient Temperature,” or ASTM E1112, “Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature,” or ASTM E1104, “Standard Specification for Clinical Thermometer Probe Covers and Sheaths”) must validate specifications and performance of the device.
Predicate Devices
Digital Thermometers, Models: DMT series (K163518)
Submission Summary (Full Text)
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Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
November 18, 2019
Joytech Healthcare Co., LTD Mr. Ren Yunhua General Manager No. 365 Wuzhou Road, Yuhang Economic Development Zone Hangzhou City Zhejian, 311100 China
Re: K183393
Trade/Device Name: Digital Thermometer DMT series (DMT-101, DMT-411, DMT-301, DMT-102, DMT-202, DMT-412, DMT-423, DMT-433, DMT-455, DMT-108, DMT-418, DMT-106. DMT-206. DMT-416. DMT-427. DMT-437. DMT-4218. DMT-4318. DMT-1019, DMT-2019, DMT-4119, DMT-4220, DMT-4320, DMT-4340, DMT-4343, DMT-4139, DMT-2021, DMT-4121, DMT-209, DMT-1030, DMT-2030, DMT-4130, DMT-1031, DMT-2031, DMT-4131, DMT-4226, DMT-4326, DMT-4726, DMT-1027, DMT-2027, DMT-4127, DMT-1032, DMT-2032, DMT-3032, DMT-4132, DMT-3033, DMT-4233, DMT-4333, DMT-4235, DMT-4335, DMT-4735, DMT-4236, DMT-4336, DMT-3018, DMT-4238, DMT-4338)
Regulation Number: 21 CFR 880.2910 Regulation Name: Clinical Electronic Thermometer Regulatory Class: Class II Product Code: FLL Dated: October 14, 2019 Received: October 17, 2019
Dear Mr. Ren Yunhua:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
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If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4. Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
for Geeta Pamidimukkala Acting Assistant Director DHT3C: Division of Drug Delivery and General Hospital Devices, and Human Factors OHT3: Office of Gastrorenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
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## Indications for Use
510(k) Number (if known) K183393
#### Device Name
Digital Thermometer DMT series(DMT-101.DMT-411.DMT-301.DMT-202.DMT-412.DMT-423.DMT-433.DMT-455.DMT-108.DMT-418.DMT-106.DMT-416.DMT-427.DMT-437.DMT-4218.DMT-4318.DMT-1019,DMT-2019,DMT-4119,DMT-4220,DMT-4320,DMT-4340,DMT-4343,DMT-4139,DMT-4121,DMT-209,DMT-1030,DMT-2030,DMT-4130,DMT-1031,DMT-4131,DMT-4226,DMT-4326,DMT-4726,DMT-1027,DMT-2027,DMT-4127,DMT-1032,DMT-2032,DMT-4132,DMT-3033,DMT-4233,DMT-4233,DMT-4235,DMT-4335,DMT-4735,DMT-4236,DMT-4336,DMT-3018,DMT-4238,DMT-4338)
#### Indications for Use (Describe)
The Digital Thermometers DMT series(Except DMT-455) are intended to measure the human body temperature in regular mode orally, rectally or under the arm. And the devices are reusable for clinical or home use on people of all ages, including children under 8 with adult supervision.
The device model DMT-455 is intended to measure temperature orally, and the device is reusable for clinical or home use for children less than 4 years old with adult supervision.
Type of Use (Select one or both, as applicable)
□ Prescription Use (Part 21 CFR 801 Subpart D)
区 Over-The-Counter Use (21 CFR 801 Subpart C)
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# 510(k) Summary
The assigned 510(k) number is: K183393
- 1. Date Prepared: 2019.11.18
## 2. Submitter's Identification:
Name: JOYTECH HEALTHCARE CO., LTD.
Add.:No.365, Wuzhou Road, Yuhang Economic Development Zone,
Hangzhou city, 311100 Zhejiang,China
Contact Person: Yunhua Ren
Phone: +86-571-81957767
Fax: +86-571-81957750
Email: RENYH@SEJOY.COM
## 3. Name of the Device:
Trade Name: Digital Thermometer DMT series
Model:DMT-101、DMT-411、DMT-301、DMT-102、DMT-202、DMT-412、DMT-423、 DMT-433、DMT-455、DMT-108、DMT-418、DMT-106、DMT-206、DMT-416、 DMT-427、DMT-437、DMT-4218、DMT-4318、DMT-1019、DMT-2019、 DMT-4119、DMT-4220、DMT-4320、DMT-4340、DMT-4343、DMT-4139、 DMT-2021、DMT-4121、DMT-209、DMT-1030、DMT-2030、DMT-4130、 DMT-1031、DMT-2031、DMT-4131、DMT-4226、DMT-4326、DMT-4726、 DMT-1027、DMT-2027、DMT-4127、DMT-1032、DMT-2032、DMT-3032、 DMT-4132、DMT-3033、DMT-4233、DMT-4333、DMT-4235、DMT-4335、DMT-4735、DMT-4236、DMT-4336、DMT-3018, DMT-4238、DMT-4338
Common Name: Digital Thermometer
Classification name: Clinical Electronic Thermometer
## 4. Classification Information:
Product Code: FLL
Device Class: II
Panel: 80
Regulation number:21 C.F.R.880.2910
Regulation Description: Clinical electronic thermometer
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## 5. Predicate Device Information:
The Digital Thermometers are substantially equivalent to the following devices: Digital Thermometers, Models: DMT series;
FDA 510(k)number: K 163518;
Manufactured by JOYTECH HEALTHCARE CO., LTD.
#### Intended use / Indication for Use: 6.
The Digital Thermometers DMT series(Except DMT-455) are intended to measure the human body temperature in regular mode orally, rectally or under the arm. And the devices are reusable for clinical or home use on people of all ages, including children under 8 with adult supervision.
The device model DMT-455 is intended to measure temperature orally, and the device is reusable for clinical or home use for children less than 4 years old with adult supervision.
#### 7. Device Description:
The Digital Thermometers DMT series(Except DMT-455) are used to measure the human body temperature in regular mode orally, rectally, or under the arm.The device model DMT-455 is intended to measure temperature orally.
The Digital Thermometers DMT series consists of a temperature sensor, low power consumption integrated circuit (IC), LCD display, and buzzer. The resistance of sensor changes with temperature and the IC converts the resistance to frequency and calculates the temperature according to the relation of resistance and frequency. The calculated temperature is displayed on the LCD.Only model DMT-4726 and DMT-4735 are predictive optional thermometers.The patient contacting materials are Stainless Steel,TPE and Acrylonitrile Butadiene Styrene (ABS).
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# 8.Model List
| Features | A | B | C | D | E | F | G | H | I | J | K |
|----------|---|---|---|---|---|---|---|---|-------------|------------------|----------------|
| Models | | | | | | | | | | | |
| DMT-101 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.3 x 1.8x 0.9 | Approx. 10 g |
| DMT-411 | ○ | ● | ○ | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.3 x 1.8x 0.9 | Approx. 10 g |
| DMT-301 | ○ | ● | ○ | ○ | ○ | ● | ○ | ○ | ≤60 Seconds | 12.3 x 1.8x 0.9 | Approx. 10 g |
| DMT-102 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.4 x 1.8x 1.1 | Approx. 10 g |
| DMT-202 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.4 x 1.8x 1.1 | Approx. 10 g |
| DMT-412 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.4 x 1.8x 1.1 | Approx. 10 g |
| DMT-423 | ● | ○ | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.4 x 2.4x 1.2 | Approx. 12 g |
| DMT-433 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.4 x 2.4x 1.2 | Approx. 12 g |
| DMT-455 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 5.8x 4.1x 4.3 | Approx. 13 g |
| DMT-108 | ○ | ● | ○ | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.3x 1.2 | Approx. 12 g |
| DMT-418 | ○ | ● | ○ | ● | △ | ● | ○ | ○ | ≤45 Seconds | 13.9 x 2.3x 1.2 | Approx. 12 g |
| DMT-106 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.2 x 1.9x 1.1 | Approx. 11 g |
| DMT-206 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.2 x 1.9x 1.1 | Approx. 11 g |
| DMT-416 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.2 x 1.9x 1.1 | Approx. 11 g |
| DMT-427 | ● | ○ | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.4 x 1.9x 1.1 | Approx. 11 g |
| DMT-437 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.4 x 1.9x 1.1 | Approx. 11 g |
| DMT-4218 | ● | ○ | ● | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.2x 1.3 | Approx. 11 g |
| DMT-4318 | ● | ○ | ● | ● | △ | ● | ○ | ○ | ≤45 Seconds | 13.9 x 2.2x 1.3 | Approx. 11 g |
| DMT-3018 | ● | ○ | ● | ○ | △ | ● | ○ | ○ | ≤60 Seconds | 13.9 x 2.2x 1.3 | Approx. 11 g |
| DMT-1019 | ○ | ● | ○ | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.3x 1.3 | Approx. 11 g |
| DMT-2019 | ○ | ● | ● | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.3x 1.3 | Approx. 12 g |
| DMT-4119 | ○ | ● | ● | ● | △ | ● | ○ | ○ | ≤45 Seconds | 13.9 x 2.3x 1.3 | Approx. 12 g |
| DMT-4220 | ● | ○ | ● | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.3x 1.3 | Approx. 13 g |
| DMT-4320 | ● | ○ | ● | ● | △ | ● | ○ | ○ | ≤45 Seconds | 13.9 x 2.3x 1.3 | Approx. 13 g |
| DMT-2021 | ○ | ● | ● | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 12.2 x 1.9x 1.0 | Approx. 11 g |
| DMT-4121 | ○ | ● | ● | ● | △ | ● | ○ | ○ | ≤45 Seconds | 12.2 x 1.9x 1.0 | Approx. 11 g |
| DMT-209 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.8 x 2.0x 1.2 | Approx. 11 g |
| DMT-1030 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 13.2 x 2.3x 1.2 | Approx. 11 g |
| DMT-2030 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 13.2 x 2.3x 1.2 | Approx. 11 g |
| DMT-4130 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 13.2 x 2.3x 1.2 | Approx. 11 g |
| DMT-1031 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 13.0 x 1.9x 1.0 | Approx. 12 g |
| DMT-2031 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 13.0 x 1.9x 1.0 | Approx. 12 g |
| DMT-4131 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 13.0 x 1.9x 1.0 | Approx. 12 g |
| DMT-4226 | ● | ○ | ● | ○ | △ | ○ | ○ | ○ | ≤60 Seconds | 13.5 x 3.4x 1.7 | Approx. 22 g |
| DMT-4326 | ● | ○ | ● | ● | △ | ● | ○ | ○ | ≤45 Seconds | 13.5 x 3.4x 1.7 | Approx. 22 g |
| DMT-4726 | ● | ○ | ● | ● | Δ | ● | Δ | Δ | ≤45 Seconds | 13.5 x 3.4x 1.7 | Approx. 22 g |
| DMT-1027 | ○ | ● | ○ | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.2 x1.8 x 1.1 | Approx. 10 g |
| DMT-2027 | ○ | ● | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 12.2 x1.8 x 1.1 | Approx. 10 g |
| DMT-4127 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.2 x 1.8 x 1.1 | Approx. 10 g |
| DMT-1032 | ○ | ● | ○ | ○ | Δ | ○ | ○ | ○ | ≤60 Seconds | 13.8 x 2.2 x 1.2 | Approx. 12 g |
| DMT-2032 | ○ | ● | ● | ○ | Δ | ○ | ○ | ○ | ≤60 Seconds | 13.8 x 2.2 x 1.2 | Approx. 12 g |
| DMT-3032 | ○ | ● | ● | ○ | ○ | ● | ○ | ○ | ≤60 Seconds | 13.8 x 2.2 x 1.2 | Approx. 12 g |
| DMT-4132 | ○ | ● | ● | ● | Δ | ● | ○ | ○ | ≤45 Seconds | 13.8 x 2.2 x 1.2 | Approx. 12 g |
| DMT-3033 | ● | ○ | ● | ○ | ○ | ● | ○ | ○ | ≤60 Seconds | 13.9 x 2.2x 1.2 | Approx. 12 g |
| DMT-4233 | ● | ○ | ● | ○ | Δ | ○ | ○ | ○ | ≤60 Seconds | 13.9 x 2.2x 1.2 | Approx. 12 g |
| DMT-4333 | ● | ○ | ● | ● | Δ | ● | ○ | ○ | ≤45 Seconds | 13.9 x 2.2 x 1.2 | Approx. 12 g |
| DMT-4235 | ● | ○ | ● | ○ | Δ | ○ | ○ | ○ | ≤60 Seconds | 13.4 x 3.1 x 1.6 | Approx. 23 g |
| DMT-4335 | ● | ○ | ● | ● | Δ | ● | ○ | ○ | ≤45 Seconds | 13.4 x 3.1 x 1.6 | Approx. 23 g |
| DMT-4735 | ● | ○ | ● | ● | Δ | ● | Δ | Δ | ≤45 Seconds | 13.4 x 3.1x 1.6 | Approx. 23 g |
| DMT-4236 | ● | ○ | ● | ○ | ○ | ○ | ○ | ○ | ≤60 Seconds | 13.1 x 2.0x 1.2 | Approx. 10 g |
| DMT-4336 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 13.1 x 2.0x 1.2 | Approx. 10 g |
| DMT-4343 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 14.2 x 2.3x 1.3 | Approx. 11 g |
| DMT-4238 | ● | ○ | ● | ○ | ○ | ● | ○ | ○ | ≤60 Seconds | 12.5 x 2.1x 1.2 | Approx. 12.8 g |
| DMT-4338 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 12.5 x 2.1x 1.2 | Approx. 12.8 g |
| DMT-4139 | ○ | ● | ● | ● | ○ | ● | ○ | ○ | ≤60 Seconds | 13.2 x 2.3x 1.3 | Approx. 14.5 g |
| DMT-4340 | ● | ○ | ● | ● | ○ | ● | ○ | ○ | ≤45 Seconds | 13.2 x 2.3x 1.3 | Approx. 14.5 g |
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A=Flexible tip
B=Rigid tip
C=Waterproof
D=Instant
E=TEMPERATURE ARROW INDICATING function
F=°C/°F switchable
G=Backlight function
H=Predictive
I=Water Bath Response time
J=Physical dimensions(L x H x W in cm) K=Weight(
including battery in grams )
• = Yes
o = No
△ =Optional
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# 9. Comparing to Predicate Device:
| SE Comparisons | Subject device application k183393 | Predicate device k163518<br>(Model:DMT series) | Comparison<br>Result |
|-------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------|
| Intended Use<br>/Indication for use | DMT series(except DMT-455) are<br>intended to measure the human body<br>temperature in regular mode orally,<br>rectally or under the arm. And the<br>devices are reusable for clinical or<br>home use on people of all ages.<br>including children under 8 with adult<br>supervision.<br>DMT-455 is intended to measure<br>temperature orally, and the device is<br>reusable for clinical or home use for<br>children less than 4 years old with<br>adult supervision. | DMT series(except DMT-455) are<br>intended to measure the human body<br>temperature in regular mode orally,<br>rectally or under the arm. And the<br>devices are reusable for clinical or<br>home use on people of all ages.<br>including children under 8 with adult<br>supervision.<br>DMT-455 is intended to measure<br>temperature orally, and the device is<br>reusable for clinical or home use for<br>children less than 4 years old with<br>adult supervision. | Identical |
| Measurement Site | DMT series (except DMT-455):<br>orally, rectally or under the arm<br><br>DMT-455:orally | DMT series (except DMT-455):<br>orally, rectally or under the arm<br><br>DMT-455:orally | Identical |
| Range | DMT series<br>(except DMT-30XX, DMT-47XX):<br>$32.0°C~43.9°C (90.0°F~111.9°F)$<br>DMT-301,DMT-3032,DMT-3033,<br>DMT-3018:<br>$32.00°C~43.99°C(90.00°F~111.99°F)$<br>DMT-4735,DMT-4726: $32.0°C~43.9°C (89.6°F~111.0°F)$ | DMT series<br>(except DMT-30XX,DMT-47XX):<br>$32.0°C~42.9°C (90°F~109.9°F)$<br>DMT-301,DMT-3032,DMT-3033:<br>$32.00°C~42.99°C (90.00°F~109.99°F)$<br>DMT-4735,DMT-4726: $32.0°C~42.9°C (89.6°F~109.2°F)$ | Similar |
| Accuracy | $±0.1°C$ between $35.5°C$ to<br>$42.0°C (±0.2°F,95.9°F-107.6°F)$ ,<br>$±0.2°C$ under $35.5°C$ or over<br>$42.0°C (±0.4°F$ under $95.9°F$ or over<br>$107.6°F$ )<br>DMT-301, DMT-3032, DMT-3033, DMT-<br>3018: $±0.10 °C$ between $35.5°C$ to $42°C$ | $±0.1°C$ between $35.5°C$ to<br>$42.0°C (±0.2°F,95.9°F-107.6°F)$ ,<br>$±0.2°C$ under $35.5°C$ or over<br>$42.0°C (±0.4°F$ under $95.9°F$ or over<br>$107.6°F$ ) | Identical |
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| | | DMT series(except DMT-301,<br>DMT-3032,DMT-3033,DMT-3018):<br>0.1°C/0.1 °F<br>DMT-301,DMT-3032,DMT-3033,<br>DMT-3018:0.01℃/0.01°F | DMT series(except DMT-301,<br>DMT-3032,DMT-3033):<br>0.1°C/0.1 °F<br>DMT-301,DMT-3032,DMT-3033:<br>0.01 ℃/0.01°F | Identical | |
|--------------------------------------------|--------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------|-----------|
| Display resolution | | | | | |
| components | | Sensor, buzz film, housing, stainless<br>steel cap, LCD display, measurement<br>control module. | Sensor, buzz film, housing, stainless<br>steel cap, LCD display,<br>measurement control module. | Identical | |
| Principle of operation | | A change of thermistor resistance,<br>caused by changes of temperature.<br>The resistance is measured by<br>microcontroller unit (MCU), so<br>changes of temperature will<br>correspond to changes of resistance. | A change of thermistor resistance,<br>caused by changes of temperature.<br>The resistance is measured by<br>microcontroller unit (MCU), so<br>changes of temperature will<br>correspond to changes of resistance | Identical | |
| Operating range | | Temperature: 41°F~104°F (5°C<br>~40°C) Relative humidity:<br>15%~95%RH<br>Atmospheric Pressure : 700hPa ~<br>1060hPa | Temperature: 41°F~104°F (5°C<br>~40°C) Relative humidity:<br>15%~95%RH<br>Atmospheric Pressure : 700hPa ~<br>1060hPa | Identical | |
| Patient contact<br>material | | ABS,TPE,Stainless Steel | ABS,TPE,Stainless Steel | Identical | |
| Colour coding | ABS | 9003 | ABS | 9003 | Identical |
| | TPE | P351C,P288C,P374C,P2<br>84C,P2715C,P109C,P42<br>8C,P427C | TPE | P351C,P288C,P374C,P<br>284C,P2715C,P109C,P<br>428C,P427C | |
| Storage and<br>transportation<br>condition | Temperature: | -4°F~131°F (-20℃~55℃)<br>Relative humidity: 15%~95%RH<br>Atmospheric Pressure : 700hPa ~ | Temperature: | -4°F~131°F (-20℃~55℃)<br>Relative humidity: 15%~95%RH<br>Atmospheric Pressure : 700hPa ~ | Identical |
{9}------------------------------------------------
| | 1060hPa | 1060hPa | |
|-------------------|--------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------|-----------|
| Battery type | One 1.5 V DC. button battery (size<br>LR41or SR41, UCC 392)<br>DMT-4726,DMT-4735:<br>One 3.0V CR2032 battery | One 1.5 V DC. button battery (size<br>LR41or SR41, UCC 392)<br>DMT-4726,DMT-4735:<br>One 3.0V CR2032 battery | Identical |
| Biocompatibility | Comply with ISO 10993-5 and ISO<br>10993-10 | Comply with ISO 10993-5 and ISO<br>10993-10 | Identical |
| Electrical Safety | Complied with IEC 60601-1 | Complied with IEC 60601-1 | Identical |
| EMC | Complied with IEC 60601-1-2 | Complied with IEC 60601-1-2 | Identical |
The differences between two devices are:
1. Changed thermometer chip to extend temperature measuring range from 32.0~42.9℃ to 32.0~43.9 ℃ ,as new version of standard ISO 80601-2-56:2017 required, no other functions changed.
2.New model DMT-3018: it is a new model that have same appearance and same electrical scheme with predicate device model DMT-4318 but have only different temperature range and PCB with the predictive device.
## 10. Performance data
The following performance data were provided in support of the substantial equivalence determination:
Performance testing was conducted to validate and verify that Digital Thermometers, DMT series met all requirements of related international standards, including electrical safety, EMC, biocompatibility, software validation and product specifications. Results of these tests demonstrate compliance to the requirements of the below consensus standards.
Electrical Safety and performance requirements:
- . AAMI / ANSI ES60601-1:2005/(R)2012 And A1:2012,C1:2009/(R)2012 And A2:2010/(R)2012 Medical Electrical Equipment
- ISO80601-2-56:2017 Medical electrical equipment Part 2-56 Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
- · ASTM E1112:00(Reapproved 2011) Standard specification for Electronic Thermometer for Intermittent Determination of Patient Temperature
{10}------------------------------------------------
Home-used medical equipment requirements and environmental test:
- IEC 60601-1-11:2015 General requirements for basic safety and essential performance -- Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
Electromagnetic compatibility requirements:
- IEC 60601-1-2:2014 Medical electrical equipment Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
Biocompatibility Evaluation for patient contacting components:
- · ISO 10993-5:2009 Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity
- · ISO10993-10:2010 Biological evaluation of medical devices -- Part 10: Tests for irritation and skin sensitization
#### Guidance Document:
· Guidance on the content of Premarket Notifications [510(k)] Submissions for clinical electronic thermometers
The software/firmware verification and validation was provided in accordance with the "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices," dated May 11, 2005.
## 11. Discussion of Clinical Tests Performed:
Clinical tests were conducted on the DMT-4726 and DMT-4735. The clinical tests evaluated 450 of subjects. and the thermometer was evaluated in three groups 1) infants-newborn to one year; 2) children-greater than one to five years; and 3) adults-greater than five years old.The clinical performance test protocol and data analysis were conducted in accordance with the requirement of ISO 80601-2-56. The test report showed the clinical performance of the subject devices complied with the requirement of ISO 80601-2-56.
## 12. Conclusions:
Based on the information provided in this submission,the subject digital thermometers DMT series are substantially equivalent to the predicate thermometers, model: DMT series.
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.