American Cyanamid Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Cyanamid Co. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
American Cyanamid Co. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Cyanamid Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Cyanamid Co.
7 devices
Cleared
Dec 17, 1993
FLEXON AND STAINLESS STEEL SUTURES
General & Plastic Surgery
295d
Cleared
Jul 08, 1993
DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING
General & Plastic Surgery
129d
Cleared
Nov 18, 1992
CUTTING AND COAGULATION DEVICES AND ACCESSORIES
General & Plastic Surgery
224d
Cleared
Jun 09, 1992
VALTRAC(R) INTRODUCER FORCEP
General & Plastic Surgery
21d
Cleared
Jul 05, 1990
DEXON II ABSORBABLE SURGICAL SUTURE, U.S.P.
General & Plastic Surgery
170d
Cleared
May 07, 1990
COATED NOVAFIL, POLYBUTESTER, MESH
General & Plastic Surgery
145d
Cleared
Jun 15, 1983
APPOSE SKIN STAPLER & REMOVER
General & Plastic Surgery
197d