Norton Performance Plastics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Norton Performance Plastics Corp. - FDA 510(k) Cleared Devices
39
Total
39
Cleared
0
Denied
Norton Performance Plastics Corp. has 39 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 39 cleared submissions from 1977 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Norton Performance Plastics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Norton Performance Plastics Corp.
39 devices
Cleared
Dec 09, 1985
NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000
Cardiovascular
89d
Cleared
Sep 25, 1985
ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION
Cardiovascular
77d
Cleared
May 07, 1985
CORRECT FLO
General Hospital
36d
Cleared
Sep 11, 1984
FLUID ADMINISTRATION LINE W/SPIKE 14-923
General Hospital
50d
Cleared
Jul 13, 1984
CENTRAL VENOUS CATHETER W/BIG-GARD
Cardiovascular
71d
Cleared
Apr 17, 1984
MICROFUSE INTRAVENOUS CATHETER SET
Cardiovascular
88d
Cleared
Oct 19, 1983
TEMP. REPAIR KIT-DUAL LUMEN CATHETER
General Hospital
155d
Cleared
Aug 11, 1983
DISPOSABLE PRESSURE TRANSDUCER#14004195
Cardiovascular
78d
Cleared
Apr 30, 1983
CENTRAL VEIN CATHERIZATION KIT-14-690-
Cardiovascular
47d
Cleared
Apr 28, 1983
FRENCH PERCUTANEOUS SHEATH INTRODUCER
Cardiovascular
45d
Cleared
Apr 14, 1983
PERM. REPAIR KIT FOR LEONARD NORTON DUAL
General Hospital
17d
Cleared
Jul 30, 1982
LEONARD PERIPHERAL VENOUS PRESSURE CATH
Cardiovascular
23d
Looking for a specific device from Norton Performance Plastics...? Search by device name or K-number.
Search all Norton Performance... devices