Company ยท US
Harbor Medical Devices, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1989. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 15, 1989 | K884628 | HARBORIN CENTRAL VENOUS CATHETER Harbor Medical Devices, Inc. | DQR |
| Apr 21, 1989 | K890518 | SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM Harbor Medical Devices, Inc. | LJT |
| Dec 13, 1988 | K882657 | HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT Harbor Medical Devices, Inc. | DYB |
| Jul 28, 1988 | K881884 | HARBOR CENTRAL VENOUS CATHETER Harbor Medical Devices, Inc. | DQR |
| Jun 9, 1988 | K882190 | S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM Harbor Medical Devices, Inc. | LJT |
| Feb 19, 1988 | K880297 | SEA - PORT INFUSION SET Harbor Medical Devices, Inc. | LJT |
| Jan 14, 1988 | K874414 | HYPODERMIC NEEDLES, SINGLE LUMEN Harbor Medical Devices, Inc. | FMI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||