Anchor Products Co. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Anchor Products Co. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1979 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Anchor Products Co. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Anchor Products Co.
7 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
Cleared
Mar 26, 1979
ANCHOR BRAND COUNT-TAINER
General Hospital
28d