Namic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Namic - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Namic
8 devices
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