Harbor Medical Devices, Inc.
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| HARBORIN CENTRAL VENOUS CATHETER (K884628) | Harbor Medical Devices, Inc. | 1989-05-15 |
| SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM (K890518) | Harbor Medical Devices, Inc. | 1989-04-21 |
| HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT (K882657) | Harbor Medical Devices, Inc. | 1988-12-13 |
| HARBOR CENTRAL VENOUS CATHETER (K881884) | Harbor Medical Devices, Inc. | 1988-07-28 |
| S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM (K882190) | Harbor Medical Devices, Inc. | 1988-06-09 |
| SEA - PORT INFUSION SET (K880297) | Harbor Medical Devices, Inc. | 1988-02-19 |
| HYPODERMIC NEEDLES, SINGLE LUMEN (K874414) | Harbor Medical Devices, Inc. | 1988-01-14 |
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