VITALOGRAPH HAND HELD SPIROMETER, MODEL 2120
Device Facts
| Record ID | K100687 |
|---|---|
| Device Name | VITALOGRAPH HAND HELD SPIROMETER, MODEL 2120 |
| Applicant | Vitalograph (Ireland) , Ltd. |
| Product Code | BZG · Anesthesiology |
| Decision Date | Oct 16, 2010 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 868.1840 |
| Device Class | Class 2 |
Indications for Use
The device is a battery operated spirometer which measures three basic patient respiratory parameters {FVC, MVV and VC}. The model 2120 is a hand held spirometer designed for lung function testing in a variety of environments such as hospital wards, health centres and private homes. The model 2120 can be configured as a stand-alone spirometer or connected to a printer.
Device Story
Hand-held, battery-operated diagnostic spirometer; measures respiratory parameters (FVC, MVV, VC) using Fleisch Pneumotachograph flowhead. Used in hospitals, clinics, and homes by clinicians or patients. Input: patient breath flow; Output: lung volumes and flow rates displayed on LCD or optional touchscreen. Data stored on-device (up to 1,000 tests/10,000 subjects) for later printing or export via USB/Micro SD to Spirotrac software. Upgraded ergonomics and user interface from predicate; maintains established measurement principles. Benefits include portable, simple assessment of respiratory function to aid clinical decision-making.
Clinical Evidence
Bench testing only. Device performance validated against ATS/ERS 2005, ISO 23747:2007, and EN ISO 26782:2009 standards. Electrical safety and EMC/EMI testing performed per IEC 60601-1 and 60601-1-2. Accuracy metrics reported as +/- 3% for FEV1/FEV6 and +/- 5% for PEF.
Technological Characteristics
Handheld, battery-powered (2 x 1.5v AAA). Fleisch Pneumotachograph sensing principle. Materials: PC/ABS, silicone rubber, stainless steel. Connectivity: USB, Micro SD card. Interface: Button keypad or optional touchscreen. Dimensions: 160 x 100 x 45 mm. Weight: 230g. Standards: ATS/ERS 2005, ISO 23747:2007, EN ISO 26782:2009, IEC 60601.
Indications for Use
Indicated for patients requiring pulmonary function testing to measure respiratory parameters including FVC, MVV, and VC. Designed for use in hospital wards, health centers, and private homes.
Regulatory Classification
Identification
A diagnostic spirometer is a device used in pulmonary function testing to measure the volume of gas moving in or out of a patient's lungs.
Predicate Devices
Reference Devices
- Vitalograph Compact (K854526)
- Vitalograph Alpha (K873562)
- Vitalograph Escort (K925085)
- Spirotrac (K912412)
- KoKo Legend (K051572)
- SpiroPro (K031515)
Submission Summary (Full Text)
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## 510K Summary
# K100687
### as required by 21 CFR 807.92
## OCT 1 6 2010
- 1. Company Information: Name: Vitalograph (Ireland) Ltd Address: Gort Road Business Park, Ennis, Co Clare, Ireland:
Tel: +353656864100 Fax: +353656829289.
- 2. Contact Person / Official Correspondent: Mr. Tom J Healy Regulatory Affairs / Quality Assurance Manager
- 3. Date of Submission: January 25th 2010.
- 4. Device Trade Name: Vitalograph Model 2120
- 5. Common / Usual name: Hand Held Spirometer,
- 6. Classification number: Spirometer as classified in Class II per 21 CFR 868.1840
Extracted from 21 CFR 868 on September 28, 2007:
#### Subpart B -- Diagnostic Devices
- Sec. 868.1840 Diagnostic spirometer.
- (a) Identification. A diagnostic spirometer is a device used in pulmonary function testing to measure the volume of gas moving in or out of a patient's lungs.
- (b) Classification. Class II (performance standards).
7. Predicate Device:
| Manufacturer | : Vitalograph |
|--------------|-----------------------------|
| Device Name | : 2120 Hand Held Spirometer |
| 510(k) No | : K946075 |
| Manufacturer: | Cardinal Health |
|---------------|-----------------|
| Device Name: | SpiroPro |
| 510(k) No: | K092324 |
8. Description of Device:
The Vitalograph Model 2120 is intended to be used, as its predecessor, as a battery operated spirometer which measures three basic patient respiratory parameters {FVC,
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MVV and VC}. The model 2120 is a hand held spirometer designed for lung function testing in a variety of environments such as hospital wards, health centres and private homes. The model 2120 can be configured as a stand-alone spirometer or connected to a printer.
The Model 2120 series has been available to the marketplace for over 15 years {ref K946075}. This device is a hand held electronic Spirometer, used in the simple assessment of respiratory function through the measurement of dynamic lung volumes i.e. Spirometry. This revised design is an upgrade to the existing product in terms of modernising its look and feel {i.e. changes to ergonomics and user interface}. The intended uses and operating principles in relation to its measurement of respiratory function remain unchanged.
Its primary functions are:
- 1. Spirometry measurements using single breath and multiple-breath testing techniques, the display and recording of measured lung volumes and flow rates (including FVC, VC, MVV) and it's subdivisions,
- 2. Record subject data. Storage of data and test results on unit for later printing or export to Spirotrac {see K912412}.
- 3. The flowhead will be a Fleisch Pneumotachograph type flowhead, the operating principle of which has been well established in the existing Model 2120 {K946075} and various other spirometers. {e.g. Vitalograph Compact Ref K854526. Vitalograph Alpha ref K873562, Vitalograph Escort K925085}
All variants of the Model 2120 {e.g. including In2itive, e-Diary} will use very same operating principle, LCD, Buttons, optional Touchscreen, and Mouldings. Items that may vary within the range are the list of parameters that the different variants display.
Navigation is allowed via the use of five buttons {Up, Down, Enter/Select, Cancel /Esc and power On/Off} or an optional touch screen.
9. Intended use:
The device is a battery operated spirometer which measures patient respiratory parameters. The model 2120 is a hand held spirometer designed for lung function testing in a variety of environments such as hospital wards, health centres and private homes. The model 2120 can be configured as a stand-alone spirometer or connected to a printer.
10. Technological Characteristics
The Vitalograph Model 2120, as with its predecessor, the Vitalograph 2120, uses a Fleisch Pneumotachograph to measure lung function. These are intended to be handheld, portable devices. All are battery powered, with charging, and button operated.
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The primary difference between the revised 2120 Hand Held Spirometer and the Vitalograph predicate device is the inclusion of an optional touch screen for navigating the simple icon driven menus along with the existing buttons and the inclusion of USB communication, where the predicate used serial communication, for data export / printing. An increase in memory in the proposed device to allow the storage of more tests and subjects {up to 1,000 tests and 10.000 subjects} is also in place. The memory continues to be of the same type as the predicate but allows for an increase in storage due to the larger capacities currently available.
Both proposed and predicate Vitalograph devices continue to use a Fleisch Pneumotachograph in their flowhead design, they both have simple button navigation options {Up, Down, Power On-Off, Del / Cancel} and they both are handheld, battery powered devices that have a charging cradle.
The use of Touchscreen interface, whilst newly incorporated into the Vitalograph proposed design, is currently available in the other predicate devices listed, as well as the pneumotach measuring principle.
There has been no change to the operating principle used by either the submitted device or its predicate. The flowhead will be a Fleisch Pneumotachograph type flowhead, the operating principle of which has been well established in the existing Model 2120 {K946075} and various other Vitalograph spirometers. {E.g. Vitalograph Compact Ref K854526, Vitalograph Alpha ref K873562, Vitalograph Escort K925085}.
Safety and effectiveness have been assured through the extensive testing in relation to IEC 60601 standards for electrical safety and EMC/EMI, as well as device specific performance testing to American Thoracic Society {ATS}and International Organisation for Standardisation {ISO} standards.
| | Vitalograph Model<br>2120<br>Specifications | Predicate Device -<br>Vitalograph 2120<br>Specifications -<br>K946075 | Predicate Devices -<br>KoKo Legend<br>K051572 | Predicate<br>Devices -<br>SpiroPro<br>K092324 /<br>K031515 |
|-----------------------------------------------|---------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------|---------------------------------------------------------------------------------------|
| Volume Range: | 0-10 Litres | 0-8Litres | | 0.1 - 8 Litres |
| Max Flow Range | 0-16 Litres / second | 0-16 Litres / second | 16 Litres / second | 0.1-16 Litres /<br>second |
| Back Pressure | Less than 0.1kPa/L/s | 0.1kPa/L/s | 1.5 cmH20/l/s | Maximum 2kPa at 15<br>L/s |
| Accuracy FEV1: | +/- 3% | +/- 3% | +/- 3% | +/- 3% |
| Accuracy FEV6 | +/-3% | +/- 3% | +/- 3% | +/- 3% |
| Accuracy PEF | +/-5% | +/-5% | | +/- 5% |
| Calibration | Using calibration<br>syringe | Using calibration<br>syringe | Using calibration syringe | Using calibration<br>syringe |
| Technology: | Fleisch<br>Pneumotachograph | Fleisch<br>Pneumotachograph | Pneumotach | Pneumotach |
| Set Predicted /<br>reference values | Yes | Yes | Yes | Yes |
| Memory Type /<br>Storage: | Yes, Non-volatile data storage | Yes, Non-volatile data<br>storage | Not available | Yes, Non-volatile<br>data storage |
| Sounds: | Audible beeps emitted<br>during power on,<br>whilst performing a<br>test, at end of test and<br>for each key press. | Audible beeps emitted<br>during power on, whilst<br>performing a test, at<br>end of test and for each<br>key press. | Not available | Not available |
| Communication: | USB, Micro SD card | Serial | RJ45, Serial | Serial, Bluetooth |
| Export of data to<br>Spirotrac<br>(K912412) | Yes | Yes | Not to Spirotrac, but does<br>export to its own<br>KoKoPFT windows PC<br>software | Not to Spirotrac, but<br>does export to its<br>own SpiroPro<br>windows PC<br>software |
| To be serviced | Yes, Service<br>Manuals. | Yes, via Service<br>Manuals. | Not available | Not available |
| Connection to<br>external printer | Yes | Yes | Yes | Yes |
| Battery Warnings:<br>Battery Type<br>{power}: | On-screen Battery<br>Low, and Battery<br>Icon {Flashing icon}<br>3v, 2 x 1.5v AAA | Low Battery warning<br>and audible beeps.<br>3v Li coin cell (CR2450) | 12v DC | 3.7v Li ion battery |
| Autopowerdown | 2-10minutes | 2 minutes | Not available | Not available |
| Dimensions: | 160 x 100 x 45 mm | 215 x 130x 70 mm | 235 x 254 x 70mm | 150 x 96 x 40mm |
| Weight: | Device Incl batteries<br>230g. | Device Incl batteries<br>520g. | 1600g | 200g including<br>battery |
| Material Type: | PC/ABS, Silicone<br>Rubber, Stainless<br>Steel, | PC/ABS, TPX, Acetal,<br>Polyester, Aluminium,<br>Stainless Steel | Not available | Rotec ABS 1001FR<br>VO |
| Operating Temp: | 10-40°C.<br>{At least 17-37°C<br>required per ATS<br>2005} | 5 to 40°C | 10-40°C | Compliant with<br>ATS |
| Storage Temp: | 0 - 50 °C | 0 - 50 °C | -20 to 70°C | Not available |
| Humidity: | 10 - 95% relative<br>humidity | 10 - 95% relative<br>humidity | 10 - 90% relative humidity | Not available |
| Performance<br>Standards: | ATS ERS 2005, ISO<br>23747:2007 for PEF<br>{formerly<br>EN13826:2003}, EN<br>ISO 26782:2009 | ATS & ERS {now<br>combined into ATS /<br>ERS 2005} | ATS / ERS 2005 | ATS / ERS 2005 |
| Compliance: | IEC / EN 60601 {EN<br>60601-1-1 and EN<br>60601-1-2} | IEC / EN 60601 {EN<br>60601-1-1 and EN<br>60601-1-2} | IEC / EN 60601 {EN<br>60601-1-1 and EN 60601-<br>1-2} | Not available |
| Interface with user | Button keypad /<br>Touchscreen | Button Keypad | Touchscreen | TouchScreen |
| Regulatory: | FDA - 510(k)<br>CE {0086} Class 2a | FDA - 510(k)<br>CE {0086} Class 2a | FDA 510K<br>CE{0086} | FDA 510K<br>CE {0123} |
| Warranty: | 1 Year | 1 Year | Not available | Not available |
Table 1. Comparison with Predicate.
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#### Conclusion:
The characteristics of the Model 2120 is similar to those of the Vitalograph predicate device listed in Table 1 above. The similarities are
- . Same intended use
- . Some operating principle
- Same spirometry parameters .
- Same algorithm for spirometry parameters calculation. .
- Same physical characteristics & method of use. .
The characteristics of the Model 2120 is similar to those of the other predicate devices listed in Table 1 above. The similarities are
- Touchscreen interface with the user incorporated in proposed Model 2120 . device is also incorporated into predicate devices.
- Proposed device is also a diagnostic spirometer in line with predicate devices. .
- Pneumotach principle for measurement is employed in all predicate devices. .
- . Operating temperature, storage temperatures and relative humidity ranges are similar for proposed and predicate devices in line with ATS requirements.
Based on the above, including the successful completion of all device testing, Vitalograph conclude that this device is substantially equivalent to the legally marketed predicate devices and is safe and effective for use. No new risks have been introduced by the revised design.
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Image /page/5/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized graphic of three abstract human figures in a row, with the figures appearing to be in motion. The figures are black and are set against a white background. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the graphic.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Mr. Tom J. Healv Regulatory Affairs/Quality Assurance Manager Vitalograph (Ireland) Limited Gort Road Business Park Ennis, Co Clare, Ireland
OCT 1 6 2010
Re: K100687
Trade/Device Name: Vitalograph Model 2120-Hand Held Spirometer Regulation Number: 21 CFR 868.1840 Regulation Name: Diagnostic Spirometer Regulatory Class: II Product Code: BZG Dated: October 11, 2010 Received: October 14, 2010
Dear Mr. Healy:
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. 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.
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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 (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to
http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHQffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely vours.
Sincerely yours,
Anthony D. Watson, B.S., M.S., M.B.A. Director
Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
#### Enclosure
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K100687 OCT 1 6 2010
Indications for Use
510(k) Number (if known): K100687
Device Name: Vitalograph Model 2120 - Hand Held Spirometer
Indications for Use:
The device is a battery operated spirometer which measures three basic patient respiratory parameters {FVC, MVV and VC}. The model 2120 is a hand held spirometer designed for lung function testing in a variety of environments such as hospital wards, health centres and private homes. The model 2120 can be configured as a stand-alone spirometer or connected to a printer.
Prescription Use X (Part 21 CFR 801 Subpart D) Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
AND/OR
Concurrence of CDRH, Office of Device Evaluation (ODE)
Mark J. Vitale
(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices
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510(k) Number: K100687
