Ocean Medical Products, Ltd.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K882013 | SOFT TISSUE BIOPSY DEVICE | DWO | 1988-06-15 | View |
| 510(k) | K870896 | NOTCH-NEEDLE, WESCOTT STYLE | GAA | 1987-03-18 | View |
| 510(k) | K843719 | SINGLE WALL INTRODUCER NEEDLE | DYB | 1984-10-18 | View |
| 510(k) | K823693 | MYELOGRAPHY NEEDLE | FMI | 1983-02-07 | View |
| 510(k) | K823692 | SPINAL NEEDLE | BSP | 1983-01-07 | View |
| 510(k) | K813462 | MADAYAG TYPE NEEDLE | KNW | 1982-03-01 | View |
| 510(k) | K813448 | POTTS-COURNAND STYLE NEEDLE | GAA | 1982-01-07 | View |
| 510(k) | K813460 | CHIBA SKINNY NEEDLE | GAA | 1982-01-07 | View |
| 510(k) | K813461 | PERCUTANEOUS ENTRY NEEDLE, SELDINGER | DRE | 1981-12-29 | View |
No matching devices.
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