Medical Device Manufacturer · US , Memphis , TN

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

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Innervision, Inc. has 6 FDA 510(k) cleared medical devices. Based in Memphis, US.

Historical record: 6 cleared submissions from 1994 to 1999. Primary specialty: General & Plastic Surgery.

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

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

6 devices

1-6 of 6