Medical Device Manufacturer · US , Medford , NJ

Viva-Tek Assoc., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Total

Cleared

Denied

Viva-Tek Assoc., Inc. has 2 FDA 510(k) cleared medical devices. Based in Medford, US.

Historical record: 2 cleared submissions from 1993 to 1994. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Viva-Tek Assoc., Inc.

2 devices

1-2 of 2