Medical Device Manufacturer · US , Walker , MI

Vitatek - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1981

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vitatek Cardiovascular ✕

2 devices

1-2 of 2

Cleared Nov 30, 1982

THE 500 MONITOR SERIES

Cardiovascular · 43d

Cleared Apr 03, 1981

SQUINN VITATEK 500 SERIES PHYSIOL. MONI

Cardiovascular · 14d