Medical Device Manufacturer · US , Mountain View , CA

Oxigraf, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Total

Cleared

Denied

Oxigraf, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Anesthesiology.

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

Oxigraf, Inc. is one of 7330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Oxigraf, Inc.

1 devices

1-1 of 1