Medical Device Manufacturer · US , Sylmar , CA

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

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Augerscope, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sylmar, US.

Historical record: 2 cleared submissions from 1987 to 1987. Primary specialty: Anesthesiology.

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

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

2 devices

1-2 of 2