American Seal Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Seal Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
American Seal Co. has 6 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 6 cleared submissions from 1989 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by American Seal Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Seal Co.
6 devices
Cleared
Sep 09, 1997
BOUFFANT CAP
General Hospital
91d
Cleared
Sep 09, 1997
SHOE COVER
General & Plastic Surgery
88d
Cleared
May 27, 1997
NON-STERILE ISOLATION GOWN
General Hospital
82d
Cleared
Feb 14, 1997
AMSEAL SURGICAL FACE MASK
General Hospital
105d
Cleared
May 31, 1989
MAYTEX NON-STERILE LATEX EXAM GLOVE
General Hospital
51d
Cleared
May 25, 1989
MAYTEX PATIENT EXAMINATION GLOVES
General Hospital
45d