Acutek Adhesive Specialties, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acutek Adhesive Specialties, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Acutek Adhesive Specialties, Inc. has 5 FDA 510(k) cleared medical devices. Based in Inglewood, US.
Historical record: 5 cleared submissions from 1994 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Acutek Adhesive Specialties, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Acutek Adhesive Specialties, Inc.
6 devices
Cleared
Oct 21, 1998
ACUTEK'S HYDROCOLLOID WOUND DRESSING, TIB 197013
General & Plastic Surgery
295d
Cleared
Oct 13, 1998
ACUTEK'S HYDROCOLLOID WOUND DRESSING, TIB 997002
General & Plastic Surgery
287d
Cleared
Oct 13, 1998
ACUTEK'S HYDROCOLLOID WOUND DRESSING, TIB 197012
General & Plastic Surgery
287d
Cleared
Sep 09, 1996
ACUTEK'S CLEARPASAGE
Ear, Nose, Throat
84d
Cleared
Jul 03, 1995
ACUTEK'S CLEARPASSAGE
Ear, Nose, Throat
84d
Cleared
Sep 12, 1994
TRANSPARENT DRESSING
General & Plastic Surgery
77d