U.S. Mfg. & Management, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U.S. Mfg. & Management, Inc. - FDA 510(k) Cleared Devices
5
Total
3
Cleared
0
Denied
U.S. Mfg. & Management, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 3 cleared submissions from 1984 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by U.S. Mfg. & Management, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U.S. Mfg. & Management, Inc.
5 devices
Cleared
Apr 02, 1992
CONTROLLED PASSIVE MOTION MACHINE
Physical Medicine
37d
Cleared
Jan 05, 1988
FLUID SAMPLING PACK
Hematology
69d
Cleared
Jul 24, 1986
MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT
General & Plastic Surgery
35d
Cleared
Aug 30, 1985
I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI
General & Plastic Surgery
29d
Cleared
Sep 24, 1984
VENI-SHIELD
General Hospital
56d