James River Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
James River Corp. - FDA 510(k) Cleared Devices
15
Total
14
Cleared
0
Denied
James River Corp. has 14 FDA 510(k) cleared general hospital devices. Based in Walker, US.
Historical record: 14 cleared submissions from 1983 to 1989.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - James River Corp.
15 devices
Cleared
Sep 15, 1989
COTOLIN DRAIN SPONGE AND DRESSING SPONGE
General & Plastic Surgery
58d
Cleared
Aug 09, 1989
VISULIN TRANSPARENT ADHESIVE DRESSING
General & Plastic Surgery
56d
Cleared
Jul 14, 1989
CARETOUCH EXAMINATION GLOVES
General Hospital
95d
Cleared
Jul 14, 1989
ISOLATION MASKS
General Hospital
44d
Cleared
Jul 14, 1989
MODIFIED LABELING OF SURGICAL GLOVES
General Hospital
38d
Cleared
Apr 20, 1989
JAMES RIVER BIOGEL POWDERLESS SURGICAL GLOVES
General Hospital
80d
Cleared
Oct 21, 1988
CARETEX CENTRAL SUPPLY WRAP
General Hospital
44d
Cleared
Oct 13, 1988
CARETEX OR TOWEL
General Hospital
14d
Cleared
Sep 15, 1988
SKID RESISTANT, LONG LASTING SHOE COVERS
General Hospital
20d
Cleared
Feb 24, 1988
CARETEX SURGEON'S HOODS
General Hospital
23d
Cleared
Feb 24, 1988
CARETEX SURGEON'S CAPS
General & Plastic Surgery
19d
Cleared
Jan 29, 1988
CARETEX SKID RESISTANT SHOE COVERS
General Hospital
17d
Cleared
Dec 24, 1986
CARETEX SHOE COVERS
General Hospital
35d
Cleared
Dec 09, 1986
CARETEX ISOLUTION GOWNS
General Hospital
26d
Cleared
Jan 07, 1983
CENTRAL SUPPLY ROOM WRAP
General Hospital
39d