Marwood Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marwood Medical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Marwood Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 7 cleared submissions from 1984 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Marwood Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Marwood Medical, Inc.
7 devices
Cleared
May 22, 1985
EYE PROCEDURE PACK
Ophthalmic
114d
Cleared
Mar 25, 1985
EMERGENCY ROOM PACK
General & Plastic Surgery
56d
Cleared
Mar 12, 1985
SPECIAL PROCEDURES PACK
General Hospital
43d
Cleared
Feb 25, 1985
CARDIAC CATHETERIZATION PACK
Cardiovascular
28d
Cleared
Feb 25, 1985
CARDIOVASCULAR SET UP
Cardiovascular
28d
Cleared
May 30, 1984
TPN/CVP DRESSING CHANGE KIT
General Hospital
106d
Cleared
Mar 27, 1984
I.V. START KIT
General Hospital
42d