Harbor Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K884628 | HARBORIN CENTRAL VENOUS CATHETER | May 15, 1989 |
| K890518 | SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM | April 21, 1989 |
| K882657 | HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT | December 13, 1988 |
| K881884 | HARBOR CENTRAL VENOUS CATHETER | July 28, 1988 |
| K882190 | S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM | June 9, 1988 |
| K880297 | SEA - PORT INFUSION SET | February 19, 1988 |
| K874414 | HYPODERMIC NEEDLES, SINGLE LUMEN | January 14, 1988 |