American Mcgaw is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Mcgaw - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
American Mcgaw has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1981 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by American Mcgaw Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Mcgaw
13 devices
Cleared
Nov 12, 1985
MCGAW/DROP WATCH FLOW MONITOR
General Hospital
78d
Cleared
Jan 14, 1985
ADD-A-VIAL SOLUTION TRANSFER DEVICE
General Hospital
119d
Cleared
Nov 28, 1984
MIXING CONTAINER
General Hospital
50d
Cleared
Jun 01, 1984
ACCUPRO ENTERAL FEEDING PUMP
General Hospital
37d
Cleared
Mar 06, 1984
CONCENTRATED PLATELET ADMIN. SET
General Hospital
47d
Cleared
Mar 06, 1984
PAB IV CONTAINER
General Hospital
36d
Cleared
Jun 24, 1983
CAPD - CATHETER ADAPTER
Gastroenterology & Urology
28d
Cleared
Dec 30, 1982
ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.
Physical Medicine
156d
Cleared
Apr 06, 1982
MCGAW FAT EMULSION SET
General Hospital
78d
Cleared
Dec 31, 1981
ACCUPRO I.V. ADMINISTRATION SET
General Hospital
59d
Cleared
May 08, 1981
CAPD CATHETER ADAPTER
Gastroenterology & Urology
56d
Cleared
Apr 08, 1981
I.V. ADMINISTRATION SET
Gastroenterology & Urology
19d