Harbor Medical Devices, Inc.
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) | K884628 | HARBORIN CENTRAL VENOUS CATHETER | DQR | 1989-05-15 | View |
| 510(k) | K890518 | SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM | LJT | 1989-04-21 | View |
| 510(k) | K882657 | HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT | DYB | 1988-12-13 | View |
| 510(k) | K881884 | HARBOR CENTRAL VENOUS CATHETER | DQR | 1988-07-28 | View |
| 510(k) | K882190 | S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM | LJT | 1988-06-09 | View |
| 510(k) | K880297 | SEA - PORT INFUSION SET | LJT | 1988-02-19 | View |
| 510(k) | K874414 | HYPODERMIC NEEDLES, SINGLE LUMEN | FMI | 1988-01-14 | View |
No matching devices.
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