Anchor Products Co.
Anchor Products Co. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 23, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Known Names
anchor products company, anchor products
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K091930 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB | September 23, 2009 |
| K061555 | ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM | August 31, 2006 |
| K982073 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM | September 22, 1998 |
| K884862 | ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE | December 27, 1988 |
| K873124 | ANCHOR BIOPSY NEEDLE | September 8, 1987 |
| K831648 | ANCHOR BRAND SURGICAL NEEDLES | August 16, 1983 |
| K790405 | ANCHOR BRAND COUNT-TAINER | March 26, 1979 |