Anchor Products Co. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anchor Products Co. General & Plastic Surgery ✕
6 devices
Cleared
Sep 23, 2009
ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB
General & Plastic Surgery
85d
Cleared
Aug 31, 2006
ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
General & Plastic Surgery
87d
Cleared
Sep 22, 1998
ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM
General & Plastic Surgery
102d
Cleared
Dec 27, 1988
ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE
General & Plastic Surgery
36d
Cleared
Sep 08, 1987
ANCHOR BIOPSY NEEDLE
General & Plastic Surgery
29d
Cleared
Aug 16, 1983
ANCHOR BRAND SURGICAL NEEDLES
General & Plastic Surgery
85d