Who is the manufacturer of Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H?

Shenzhen Osto Technology Company Limited filed the 510(k) submission for Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H (K210756).

What is the FDA product code for Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H?

NUH. It is classified under 21 CFR 882.5890 as a Class 2 device in the Neurology panel.

What is the regulatory pathway for Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H?

510(k) clearance (submission type: Traditional).

What are the predicate devices for Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H?

Neck Care Therapy, Models: SYK-509B (K172897); Health Expert Electronic Stimulator (model: AST-300L) (K190783).

Who can help prepare an FDA 510(k) submission like Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H

K210756 · Shenzhen Osto Technology Company Limited · NUH · Jun 11, 2021 · Neurology

Device Facts

Record ID	K210756
Device Name	Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H
Applicant	Shenzhen Osto Technology Company Limited
Product Code	NUH · Neurology
Decision Date	Jun 11, 2021
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 882.5890
Device Class	Class 2
Attributes	Therapeutic

Indications for Use

To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back of neck, back, arm, and leg, due to strain from exercise or normal household and work activities. - Neck Pad is used on back of neck. - Meridian Pad is used on shoulder, waist, back, arm and leg.

Device Story

Household multifunctional device for pain relief; uses low-frequency electrical stimulation and circular traction vibration. Inputs: user-selected pulse modes, intensity levels (50 levels), and heating levels (3 levels) via remote control or main unit buttons. Outputs: electrical pulses delivered through electrode pads or neck pad; heating. Used in home setting by patient. Healthcare provider does not operate; output used by patient to manage muscle pain. Benefits: temporary pain relief via nerve stimulation and heat.

Clinical Evidence

Bench testing only. Evaluated for electrical safety (IEC 60601-1-11, IEC 60601-2-10), electromagnetic compatibility (IEC 60601-1-2), usability (IEC 62366), and software validation. Biocompatibility of electrode/neck pads confirmed via ISO 10993-5 and ISO 10993-10 testing, noting identity to previously cleared predicate components.

Technological Characteristics

Transcutaneous electrical nerve stimulator (TENS). Materials: ABS plastic housing, stainless steel neck pad, silica gel/conductive silicone electrode pads. Energy: 3.7Vdc lithium battery (main unit), 3Vdc AAA batteries (remote). Waveform: Pulsed, symmetric, biphasic. Connectivity: Wireless remote control. Sterilization: N/A (non-sterile). Software: Microprocessor-controlled.

Indications for Use

Indicated for temporary relief of pain in shoulder, waist, back of neck, back, arm, and leg muscles due to exercise or normal household/work strain. Over-the-counter use.

Regulatory Classification

Identification

A transcutaneous electrical nerve stimulator for pain relief is a device used to apply an electrical current to electrodes on a patient's skin to treat pain.

Predicate Devices

Neck Care Therapy, Models: SYK-509B (K172897)
Health Expert Electronic Stimulator (model: AST-300L) (K190783)

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA logo on the right. The FDA logo is in blue and includes the letters "FDA" followed by the words "U.S. FOOD & DRUG ADMINISTRATION" stacked on top of each other. June 11, 2021 Shenzhen OSTO Technology Company Limited % Cassie Lee Submission Correspondent Guangzhou GLOMED Biological Technology Co., Ltd. 2231, Building 1, Rui Feng Center, Kaichuang Road, Huangpu District. Guangzhou, Guangdong, China 510663 Re: K210756 Trade/Device Name: Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H Regulation Number: 21 CFR 882.5890 Regulation Name: Transcutaneous Electrical Nerve Stimulator For Pain Relief Regulatory Class: Class II Product Code: NUH Dated: March 10, 2021 Received: March 15, 2021 Dear Ms. Lee: 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. 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. {1}------------------------------------------------ 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. Pamela Scott Assistant Director DHT5B: Division of Neuromodulation and Physical Medicine Devices OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K210756 Device Name NECK CARE THERAPY (Model: AST-905A, AST-905D, AST-905H) Indications for Use (Describe) To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, arm, and leg, due to strain from exercise or normal household and work activities. - Neck Pad is used on back of neck. - Meridian Pad is used on shoulder, waist, back, arm and leg. Type of Use (Select one or both, as applicable) |--|--| | | Prescription Use (Part 21 CFR 801 Subpart D) X Over-The-Counter Use (21 CFR 801 Subpart C) #### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ # 510(k) Summary of K210756 This summary of 510(K) safety and effectiveness information is being submitted in accordance with the requirement of 21 CFR 807.92. ## 1. Submitter's Information 510(k) Owner's Name: Shenzhen OSTO Technology Company Limited Establishment Registration Number: 3011564440 Address: No.43 Longfeng Road, Xinsheng Community, Longgang Street, Longgang District, Shenzhen City, Guangdong Province, China Tel: +86-755-29769546 Fax: +86-755-29769540 Contact Person: Li Yang (General Manager) Email: annaosto@163.com # Application Correspondent: Contact Person: Ms. Cassie Lee Guangzhou GLOMED Biological Technology Co., Ltd. Address: 2231, Building 1, Rui Feng Center, Kaichuang Road, Huangpu District, Guangzhou, Guangdong, China Tel: +86 20 8266 2446 Email: regulatory@glomed-info.com # 2. Subject Device Information Common Name: Stimulator, Nerve, Transcutaneous, Over-The-Counter, Stimulator Trade Name: NECK CARE THERAPY, Model: AST-905A, AST-905D, AST-905H Classification Name: Transcutaneous electrical nerve stimulator for pain relief, Review Panel: Neurology Product Code: NUH Regulation Number: 882.5890 Regulation Class: II # 3. Predicate Device Information Predicate Device 1: 510(K) Number: K172897 Company Name: Shenzhen OSTO Technology Co., Ltd. Address: No.43 Longfeng Road, Xinsheng Community, Longgang Street Longgang District, Shenzhen City Guangdong Province, CHINA Trade/Device Name: Neck Care Therapy, Models: SYK-509B Common Name: Electronic Stimulator Regulation Number: 882.5890 Regulatory Class: II Product Code: NUH # Predicate Device 2: 510(K) Number: K190783 Company Name: Shenzhen OSTO Technology Company Limited Address: No.43 Longfeng Road, Xinsheng Community, Longgang Street, Longgang District, {4}------------------------------------------------ Shenzhen City, Guangdong Province, China Trade/Device Name: Health Expert Electronic Stimulator (model: AST-300L) Common Name: Transcutaneous electrical nerve stimulator for pain relief Regulation Number: 882.5890, 890.5850 Regulatory Class: II Product Code: NUH, NGX ### 4. Device Description ## For Model AST-905A and AST-905H: This instrument is a new generation of a household multifunctional device based on physics, modern microelectronics and clinical practices, it uses low-frequency electronic therapy, and circular traction vibration to temporarily alleviate the pain associated with sore and aching muscles in the shoulder, waist, neck, back, arm, and leg. The main unit is used for the back of the neck and the streamlined ring design follows the physiological curvature of the human body. The Meridian Pad is used on the shoulder, waist, back, arm and leg. The device has 2 operation modes: Stimulation and heating. The stimulation has 2 modes for stimulating, and 50 output Intensity Levels. The heating only has 1 mode for heating and 3 temperature levels. The device can give a certain electrical pulse through 2 pairs of electrode pads that are placed on the skin to help users to enjoy stimulation on the shoulder, waist, back, arm, and leg when using the individual Meridian pads or on the back of the neck when using the Neck Pad. The remote control of this device is user-friendly controlled because it has the operating elements of the ON/OFF button. left or right button, and increase or decrease button. The device is equipped with accessories of electrode pads and an electrode wire. The LCD display screen can show the selected mode, the stimulation, and the time remaining of an application mode. The device can be successfully opened only when both the switch button of the remote control and the main unit turned on. When the device connected to the remote control, the remote control is the only controller to select the pulse modes, temperature modes, pulse intensity, temperature levels and adjust the treatment time. ### For Model AST-905D: This instrument is a new generation of a household multifunctional device based on physics, modern microelectronics and clinical practices, it uses low-frequency electronic therapy, and circular traction vibration to temporarily alleviate the pain associated with sore and aching muscles in the shoulder, waist, neck, back, arm, and leg. The main unit is used for the back of the neck and the streamlined ring design follows the physiological curvature of the human body. The Meridian Pad is used on the shoulder, waist, back, arm and leg. The device has 2 operation modes: Stimulation and heating. The stimulation has 2 modes for stimulating, and 50 output Intensity Levels. The heating only has 1 mode for heating and 3 temperature levels. The device can give a certain electrical pulse through 2 pairs of electrode pads that are placed on the skin to help users to enjoy stimulation on the shoulder, waist, back, arm, and leg when using the individual Meridian pads or on the back of the neck when using the Neck Pad.. The user can control the device effectively by the buttons on the main unit. There are 5 operation buttons: switch button, "M" button, ""C" button and "—" button. The switch button can help user to turn on/off the device, the "M" button intended to select the "C" button intended to select the temperature mode and the "-" button and "--" button intended to increase or decrease the Intensity Levels or temperature levels. {5}------------------------------------------------ The device is equipped with accessories of Meridian pads and an electrode wire. # 5. Intended Use / Indications for Use To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back of neck, back, arm, and leg, due to strain from exercise or normal household and work activities. - Neck Pad is used on back of neck. - Meridian Pad is used on shoulder, waist, back, arm and leg. # 6. Test Summary NECK CARE THERAPY, Model: AST-905A, AST-905D, AST-905H has been evaluated the safety and performance by lab bench testing as following: - Electrical safety test according to IEC 60601-1-11 and IEC 60601-2-10 standards � - ◆ Electromagnetic compatibility test according to IEC 60601-1-2 standard - � Usability test according to IEC 62366 standard - ◆ Software verification and validation test according to the requirements of the FDA "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices" - ◆ The waveform test has also been conducted to verify the output specifications of the device according to "Guidance for Transcutaneous Electrical Nerve Stimulator for Pain Relief Intended for Over the Counter Use and Guidance for Powered Muscle Stimulator for Muscle Conditioning". - � Biocompatibility: The body-contacting components of this device are Electrode Pads and Neck Pad. And the Electrode Pads and Neck Pad comply with biocompatibility standards ISO 10993-5 (Cytotoxicity) and ISO 10993-10 (Irritation and Sensitization) because the Electrode Pads and Neck Pad of the subject device are identical to those that had been cleared under K172897 (which clearance as K172897 on 12/07/2018) and been marketed to US market. So. we have reason to believe that the Electrode Pads and Neck Pad are safe for the users. The Electrode Pads and Neck Pad comply with the following standards. - ISO 10993-5, Biological Evaluation of Medical Devices Part 5: Tests for In Vitro Cytotoxicity; - ISO 10993-10, Biological Evaluation of Medical Devices Part 10: Tests for Irritation and Skin Sensitization. ### 7. Comparison to predicate device and conclusion The technological characteristics, features, specifications, materials, mode of operation, and intended use of NECK CARE THERAPY (Model: AST-905A, AST-905D, AST-905H) is substantially equivalent to the predicate devices quoted above. The differences between the subject device and predicate devices do not raise new issues of safety or effectiveness. | Elements of Comparison | Subject Device | Predicate Device 1 | Predicate Device 2 | Remark | | |--------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------|--------------| | Device Name and Model | NECK CARE THERAPY Model: AST-905A, AST-905D and AST- 905H | Neck Care Therapy AST-905B or SYK- 509B | Health Expert Electronic Stimulator (model: AST-300L) | -- | | | 510(k) Number | K210756 | K172897 | K190783 | -- | | | Intended Use & Indications for Use | To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back of neck, back, arm, and leg, due to strain from exercise or normal household and work activities. - Neck Pad is used on back of neck. - Meridian Pad is used on shoulder, waist, back, arm and leg. | To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back of neck, back, arm, and leg, due to strain from exercise or normal household and work activities. — Neck Pad is used in back of neck. — Meridian Pad is used in shoulder, waist, back, and arm. | PMS (Mode 1~8) It is intended to stimulate healthy muscles in order to improve and facilitate muscle performance. TENS (Mode 9~25) To be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, back of the neck, arm, leg, and foot due to strain from exercise or normal household work activities by applying current to stimulate nerve. | SE | | | Power Source(s) | Main Unit: 3.7Vdc, 2200mAh lithium battery Power Adaptor: Input: 100~240Vac, 50/60Hz, 0.2A; Output: 5Vdc, 1A Remote Control: Battery: 3Vdc, 1.5V AAA x 2 | Main Unit: Power Adaptor: Input:100~240Vac, 50/60Hz, 0.2A; Output: 5Vdc, 1A Battery: 3.7Vdc, 2200mAh Remote Control: Battery: 3Vdc, AAA x 2 Unit Input: 5Vdc, 1A | Adaptor Input: 100-240Vac, 50- 60Hz, 0.1A Output: 5Vdc, 2A Unit Input: 5Vdc, 2A | SE | | | Method of Line Current Isolation | Type BF Applied Part | Type BF Applied Part | Type BF Applied Part | SE | | | Patient Leakage Current | NC SFC | AC: 54.5μA, DC: 0.5μA AC:120.0μA, DC: 0.6μA | AC: 54.5μA, DC: 0.5μA AC:120.0μA, DC: 0.6μA | AC: 54.5μA, DC: 0.5μA AC: 120.0μA, DC: 0.6μA | SE | | Average current through electrodes when device is on but no pulses are being applied | | < 0.01μA | < 0.01μA | < 0.01μA | SE | | Number of Modes | | 3 | 2 | 25 | SE Note 1 | | Number of Output Channel | | 1 | 1 | 2 | SE | | Output Intensity Level | | For stimulating: 50 For heating: 3 | 50 steps | 99 steps | SE Note 1 | | Heating temperature | | 30-40°C | N/A | 30-40°C | SE | | Synchronous or Alternating? | | Synchronous | Synchronous | Synchronous | SE | | Method of Channel Isolation | | Voltage Transform Isolation | Voltage Transform Isolation | Voltage Transform Isolation "Body+" and "Body-" buttons for body channel, " Sole+" and "Sole-" buttons for feet channel | SE | | Regulated Current or Regulated Voltage? | | Voltage Control | Voltage Control | Voltage Control | SE | | Software/Firmware/Mi croprocessor Control? | | Yes | Yes | Yes | SE | | Automatic Overload Trip | | No | No | No | SE | | Automatic No-Load Trip | | No | No | No | SE | | Automatic Shut Off | | Yes | Yes | Yes | SE | | User Override Control | | Yes | Yes | Yes | SE | | Indicator Display | On/Off Status | Yes | Yes | Yes | SE | | | Low Battery | Yes | Yes | No | SE | | | Voltage/ Current Level | Yes | Yes | Yes | SE | | Timer Range | | 5-30 min | 5-30 min | 25 to 60 min | SE | | Weight | | | | | | | | For Main Unit: AST-905A: 193g; AST-905D: 229g; AST-905H: 178g For Electrode: Patch Electrode: 44g | Main Unit: SYK-509B: 222g Electrode: Patch Electrode: 44g | 2.1Kg (Without accessories) | SE Note 2 | | | Dimensions | | | | | | | | For Main Unit: AST-905D: $166.0*159.5*55.6$ mm AST-905H: $173.4*156.3*43.4$ mm For Electrode: Meridian Pad: $8.9*5.8$ cm Effective area: $50.04$ cm2 Neck Pad: $42.3$ mm x $29.5$ mm | Main Unit: SYK-509B: $187.2*169*67.3$ mm Patch Electrode: $8.9*5.8$ cm | $429.2$ mm x $401$ mm x $152.8$ mm | SE Note 2 | | | Housing Materials and Construction | For Electrode Pads: White silica gel, Black conductive silicone, Transparent conductive adhesive silicone, Transparent PET silicone | Electrode Pads: White silica gel, Black conductive silicone, Transparent conductive adhesive silicone, Transparent PET silicone | Main unit: ABS plastic | SE | | | | For Neck Pad: Stainless steel | Sticky metal sheet: Nickel plating | No publicly available | | | | | For Unit Housing: ABS plastic | Unit Housing: ABS plastic | No publicly available | | | | Waveform | Pulsed, symmetric, biphasic | Pulsed, symmetric, biphasic | Pulsed, symmetric, biphasic | SE | | | Shape | Rectangular, with interphase interval | Rectangular, with interphase interval | Rectangular, with interphase interval | SE | | | Maximum Output Voltage | 44V±10% @ 500Ω | 44V±10% @ 500Ω | 44V±10% @ 500Ω | SE | | | | 80V±10% @ 2KΩ | 80V±10% @ 2KΩ | 80V±10% @ 2KΩ | SE | | | | 112V±10% @ 10KΩ | 112V±10% @ 10KΩ | 112V±10% @ 10KΩ | SE | | | | | | | | | | Maximum Output Current | 88mA±10% @ 500Ω | 88mA±10% @ 500Ω | 88mA±10% @ 500Ω | SE | | | | 40mA±10% @ 2KΩ | 40mA±10% @ 2KΩ | 40mA±10% @ 2KΩ | SE | | | | 11.2mA±10% @ 10KΩ | 11.2mA±10% @ 10KΩ | 11.2mA±10% @ 10KΩ | SE | | | Pulse Duration | 120μs | 120μs | 120μs | SE | | | Pulse frequency | 77.3Hz | 77.3Hz | 77.3Hz | SE | | | Net Charge (per pulse) | 0μC @ 500Ω Method: Balanced waveform | 0μC @ 500Ω Method: Balanced waveform | 0μC @ 500Ω Method: Balanced waveform | SE | | | Maximum Phase Charge @ 500Ω | 10.56μC | 12.78μC | 10.56μC | SE | | | Maximum Average Current@ 500Ω | 1.63 mA | 0.968 mA | 1.63 mA | SE | | | Maximum Current Density (r.m.s) @ 500Ω | 0.0326 mA/cm² | 0.235 mA/cm²…

Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H

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Device Story

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Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H

Device Facts

Indications for Use

Device Story

Clinical Evidence

Technological Characteristics

Indications for Use

Regulatory Classification

Identification

Predicate Devices

Submission Summary (Full Text)

Panel 1

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