Medical Action Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Action Industries, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Medical Action Industries, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1981 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medical Action Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Action Industries, Inc.
8 devices
Cleared
Apr 25, 2005
DRAPE, SURGICAL, X-RAY ELEMENT, MODELS NON STERILE 6120-00, STERILE 704-B,...
General Hospital
220d
Cleared
Nov 08, 2004
SPATULA, CERVICAL, CYTOLOGICAL, MODEL 22-9107
Obstetrics & Gynecology
52d
Cleared
Nov 04, 2002
VAGINAL SPECULUM, MODEL 5555S, 5555M, OR 5555L
Obstetrics & Gynecology
60d
Cleared
Mar 20, 1995
SURGICLA INSTRUMENT KIT
General Hospital
98d
Cleared
Sep 11, 1992
BURN DRESSING
General & Plastic Surgery
42d
Cleared
Dec 22, 1988
GAUZE SPONGE
General & Plastic Surgery
34d
Cleared
Mar 26, 1981
SUTURE REMOVAL KIT
General & Plastic Surgery
13d
Cleared
Feb 04, 1981
LAPAROTOMY SPONGE
General & Plastic Surgery
13d