Company ยท US
Anchor Products Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 2009. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
2recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 23, 2009 | K091930 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB Anchor Products Co. | GCJ |
| Aug 31, 2006 | K061555 | ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM Anchor Products Co. | GCJ |
| Sep 22, 1998 | K982073 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM Anchor Products Co. | GCJ |
| Dec 27, 1988 | K884862 | ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE Anchor Products Co. | GES |
| Sep 8, 1987 | K873124 | ANCHOR BIOPSY NEEDLE Anchor Products Co. | GAA |
| Aug 16, 1983 | K831648 | ANCHOR BRAND SURGICAL NEEDLES Anchor Products Co. | GAB |
| Mar 26, 1979 | K790405 | ANCHOR BRAND COUNT-TAINER Anchor Products Co. | MMK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 7, 2011 | Anchor Products Company, Inc. Anchor Tissue Retrieval System; ETO sterilized, single use disposable device; port size 15 mm, 1550 mL capacity; 3 units per box; Manufacturer: Anchor Products Co., 52 Official Rd, Addison, IL 60101 U Terminated |
GCJ | K061555 |
| Mar 7, 2011 | Anchor Products Company, Inc. Anchor Tissue Retrieval System; ETO sterilized, single use disposable device; port size 10 mm, 225 mL capacity; 3 units per box; Manufacturer: Anchor Products Co., 52 Official Rd, Addison, IL 60101 U. Terminated |
GCJ | K061555 |