Medical Device Manufacturer · US , Walker , MI

Namic - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1979

Recent clearances: BREEZE DIGITAL INFLATION DEVICE, PERCEPTOR COMPENSATOR MORSE MANIFOLD

8

Total

8

Cleared

0

Denied

Namic has 8 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 8 cleared submissions from 1979 to 1996. Primary specialty: Cardiovascular.

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

Namic is one of 14669 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Namic

8 devices

1-8 of 8

Cleared Mar 29, 1996

BREEZE DIGITAL INFLATION DEVICE

Cardiovascular · 235d

Cleared Mar 25, 1996

PERCEPTOR COMPENSATOR MORSE MANIFOLD

Cardiovascular · 346d

Cleared Jul 09, 1993

MORSE ANESTHESIA MANIFOLD

General Hospital · 484d

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