Medical Device Manufacturer · US , Silver Spring , MD

Zipper Medical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Zipper Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Silver Spring, US.

Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Zipper Medical, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Zipper Medical, Inc.

1 devices

1-1 of 1