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) cleared devices by 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