Anchor Products Co.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K091930 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB | GCJ | 2009-09-23 | View |
| 510(k) | K061555 | ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM | GCJ | 2006-08-31 | View |
| 510(k) | K982073 | ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM | GCJ | 1998-09-22 | View |
| 510(k) | K884862 | ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE | GES | 1988-12-27 | View |
| 510(k) | K873124 | ANCHOR BIOPSY NEEDLE | GAA | 1987-09-08 | View |
| 510(k) | K831648 | ANCHOR BRAND SURGICAL NEEDLES | GAB | 1983-08-16 | View |
| 510(k) | K790405 | ANCHOR BRAND COUNT-TAINER | MMK | 1979-03-26 | View |
No matching devices.
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