ClearanceBrief
Company ยท US

American Cyanamid Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1993. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GDWStaple, Implantable2
FTMMesh, Surgical1
GANSuture, Absorbable, Synthetic1
GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
HJELamp, Fluorescein, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 17, 1993K930992FLEXON AND STAINLESS STEEL SUTURES
American Cyanamid Co.
GAQ
Jul 8, 1993K931056DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING
American Cyanamid Co.
GDW
Nov 18, 1992K921696CUTTING AND COAGULATION DEVICES AND ACCESSORIES
American Cyanamid Co.
GEI
Jun 9, 1992K922348VALTRAC(R) INTRODUCER FORCEP
American Cyanamid Co.
HJE
Jul 5, 1990K900198DEXON II ABSORBABLE SURGICAL SUTURE, U.S.P.
American Cyanamid Co.
GAN
May 7, 1990K896946COATED NOVAFIL, POLYBUTESTER, MESH
American Cyanamid Co.
FTM
Jun 15, 1983K823552APPOSE SKIN STAPLER & REMOVER
American Cyanamid Co.
GDW

Latest recalls

DateFirm and productCodeLinked 510(k)
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