AIRSTRIP OB

K090269 · Airstrip Technologies, LP · HGM · Feb 13, 2009 · Obstetrics/Gynecology

Device Facts

• Record ID: K090269
• Device Name: AIRSTRIP OB
• Applicant: Airstrip Technologies, LP
• Product Code: HGM · Obstetrics/Gynecology
• Decision Date: Feb 13, 2009
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 884.2740
• Device Class: Class 2
• Attributes: Software as a Medical Device, 3rd-Party Reviewed

Intended Use

AirStrip OB® is intended to be used by Obstetricians for the following purposes: To more rapidly and thoroughly respond to a nurse call regarding fetal heart tracings or maternal contraction patterns by viewing the real time waveforms remotely using a Windows-based handheld device To proactively review a fetal heart or maternal contraction tracing of a patient in Labor and Delivery for whom they are responsible but are unable to be present in the hospital at that time. To review the current Labor and Delivery patient census list. Provide a request for remote consultation regarding a fetal heart tracing. To remotely review other standard or critical real-time numeric data from Labor and Delivery.

Device Story

AirStrip OB® is a remote data viewing software for obstetricians. It receives real-time fetal heart rate and maternal contraction waveforms/numeric data from hospital Labor and Delivery monitoring systems. The software transmits this data to a Windows-based handheld device, allowing physicians to view patient tracings and census lists remotely when unable to be physically present. It facilitates rapid response to nurse calls and remote consultations. The output is a visual representation of waveforms and data on the handheld screen, enabling clinicians to make informed decisions regarding patient care and labor management. It is intended for use by obstetricians in clinical settings or remote locations.

Clinical Evidence

No clinical data provided; substantial equivalence is based on technological characteristics and intended use.

Technological Characteristics

Software-based remote data viewing system. Operates on Windows-based handheld devices. Connects to hospital Labor and Delivery monitoring systems to display real-time waveforms and numeric data. No specific hardware materials or sterilization methods applicable as it is a software-only device.

Indications for Use

Indicated for obstetricians to remotely monitor fetal heart tracings, maternal contraction patterns, and other real-time numeric data for patients in Labor and Delivery units.

Regulatory Classification

Identification

A perinatal monitoring system is a device used to show graphically the relationship between maternal labor and the fetal heart rate by means of combining and coordinating uterine contraction and fetal heart monitors with appropriate displays of the well-being of the fetus during pregnancy, labor, and delivery. This generic type of device may include any of the devices subject to §§ 884.2600, 884.2640, 884.2660, 884.2675, 884.2700, and 884.2720. This generic type of device may include the following accessories: Central monitoring system and remote repeaters, signal analysis and display equipment, patient and equipment supports, and component parts.

Submission Summary (Full Text)

{0}------------------------------------------------

## DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three stripes representing the department's mission of providing health and human services to the nation. The eagle is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA".

## Public Health Service

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

## FFB 1 3 2009

Airstrip Technologies, LP c/o Mr. Mark Job Reviewer Regulatory Technology Services, LLC 1394 25th Street, N.W. BUFFALO MN 55313

Re: K090269

> Trade/Device Name: AirStrip OB® Remote Data Viewing software Regulation Number: 21 CFR §884.2740 Regulation Name: Perinatal monitoring system and accessories Regulatory Class: II Product Code: HGM Dated: February 2, 2009 Received: February 3, 2009

Dear Mr. Job:

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.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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}------------------------------------------------

Page 2

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; good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding os substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter.

| 21 CFR 876.xxx | (Gastroenterology/Renal/Urology) | [phone] |
|----------------|----------------------------------|----------------|
| 21 CFR 884.xxx | (Obstetrics/Gynecology) | [phone] |
| 21 CFR 892.xxx | (Radiology) | [phone] |
| Other | | [phone] |

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometrics' (OSB's) Division of Postmarket Surveillance at 240-276-3474. For questions regarding the reporting of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at 240-276-3464. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufactures, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/industry.suppot/index.html.

Sincerely yours,

Janine M. Morris

Acting Director, Division of Reproductive. Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{2}------------------------------------------------

## Indications for Use Statement

| 510(k) Number | K09269 |
|---------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Device Name | AirStrip OB® Remote Data Viewing software |
| Indications for Use | AirStrip OB® is intended to be used by Obstetricians for the following purposes: <ul><li>To more rapidly and thoroughly respond to a nurse call regarding fetal heart tracings or maternal contraction patterns by viewing the real time waveforms remotely using a Windows-based handheld device</li><li>To proactively review a fetal heart or maternal contraction tracing of a patient in Labor and Delivery for whom they are responsible but are unable to be present in the hospital at that time.</li><li>To review the current Labor and Delivery patient census list.</li><li>Provide a request for remote consultation regarding a fetal heart tracing.</li><li>To remotely review other standard or critical real-time numeric data from Labor and Delivery.</li></ul> |

PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED :

Concurrence of CPP II Off oo of Devi

. '

Prescription Use X

(Per 21 CFR 801.109)

OR
Arza M Wh

(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices

510(k) Number.

Over-The-Counter Use _________________________________________________________________________________________________________________________________________________________