Carl Parker Associates, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carl Parker Associates, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Carl Parker Associates, Inc. has 7 FDA 510(k) cleared medical devices. Based in Hauppauge, US.
Historical record: 7 cleared submissions from 1987 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Carl Parker Associates, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carl Parker Associates, Inc.
7 devices
Cleared
Jun 27, 1997
DEFEND FLUID RESISTANT PLEATED MASK
General Hospital
92d
Cleared
Jan 27, 1997
COMPLEAT SURGICAL MASK
General Hospital
203d
Cleared
Jul 13, 1994
DEFEND SELF-SEALING STERILIZATION POUCH
General Hospital
441d
Cleared
Apr 26, 1989
STERILE SURGICAL GLOVES
General Hospital
48d
Cleared
Mar 22, 1989
DEFEND LATEX EXAMINATION GLOVES
General Hospital
14d
Cleared
Mar 16, 1989
DEFEND LATEX EXAMINATION GLOVES
General Hospital
10d
Cleared
Jul 22, 1987
DENTAL FACE MASKS, POLYESTER
General Hospital
91d