Associated Ent., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Associated Ent., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Associated Ent., Inc. has 4 FDA 510(k) cleared medical devices. Based in Danville, US.
Historical record: 4 cleared submissions from 1989 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Associated Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Associated Ent., Inc.
4 devices
Cleared
Oct 12, 1993
DISP MONIT POUCH /GLOVE CK PAT EXAM GLOVE LEAK DET
General & Plastic Surgery
382d
Cleared
Jul 13, 1992
GLOVE CHECK PATIENT EXAMINATION GLOVE LEAK DETECT.
General & Plastic Surgery
209d
Cleared
Jun 22, 1989
BUD BRAND PATIENT EXAMINATION GLOVES (VINYL)
General Hospital
87d
Cleared
May 12, 1989
BUD BRAND PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
46d