Medical Device Manufacturer · US , Walker , MI

Namic - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1979

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Namic Cardiovascular ✕

7 devices

1-7 of 7

Cleared Mar 29, 1996

BREEZE DIGITAL INFLATION DEVICE

Cardiovascular · 235d

Cleared Mar 25, 1996

PERCEPTOR COMPENSATOR MORSE MANIFOLD

Cardiovascular · 346d

Cleared Aug 24, 1982

HIGH PRESSURE CONTRAST INJECTION LINE

Cardiovascular · 39d

Cleared Jan 12, 1982

CONTINUOUS FLUSH DEVICE

Cardiovascular · 22d

Cleared Jan 25, 1979

ARTERIAL EXTENSION SET

Cardiovascular · 13d

Cleared Jan 25, 1979

CATHETER, ARTERIAL LINE

Cardiovascular · 13d

Cleared Jan 23, 1979

STOPCOCKS, MANIFOLDS

Cardiovascular · 36d