American White Cross, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American White Cross, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
American White Cross, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Stamford, US.
Historical record: 10 cleared submissions from 1985 to 1997.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American White Cross, Inc.
10 devices
Cleared
Feb 06, 1997
ULTRAFERA WOUND DRESSING
General & Plastic Surgery
80d
Cleared
Sep 09, 1996
AIR MAX EXTERNAL NASAL DILATOR STRIP
Ear, Nose, Throat
80d
Cleared
Jan 31, 1990
AWC BUTTERFLY WOUND CLOSURES
General & Plastic Surgery
187d
Cleared
Jan 13, 1986
WHITE CROSS STERILE PAD 4IN. X 4IN.
General & Plastic Surgery
41d
Cleared
Sep 05, 1985
DOSIMETRIC RELEASE/RADIATION STERILIZ. ABSORB GAUZ
General & Plastic Surgery
10d
Cleared
Aug 21, 1985
NON-ADHERA ADHESIVE PAD 3X4
General & Plastic Surgery
12d
Cleared
Jul 29, 1985
EXTRA LARGE ADHESIVE STRIPS
General & Plastic Surgery
53d
Cleared
Jul 29, 1985
NON-ADHERENT PAD
General & Plastic Surgery
53d
Cleared
Jul 26, 1985
TRICOT ADHESIVE BANDAGE
General & Plastic Surgery
46d
Cleared
Mar 11, 1985
3 X 4 NON-ADHERENT PAD
General & Plastic Surgery
24d