# Harbor Medical Devices, Inc.

- Location (FDA's records): Boston, MA
- FDA decisions: 7 (1988–1989): 7 510(k) clearances
- Product codes: LJT (3), DQR (2), FMI (1), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K884628: Harborin Central Venous Catheter (May 15, 1989)
- K890518: Single Lumen S.E.a.-Port Vascular Access System (Apr 21, 1989)
- K882657: Harbor S.E.a.-Port Surgical Accessory Kit (Dec 13, 1988)
- K881884: Harbor Central Venous Catheter (Jul 28, 1988)
- K882190: S.E.a.-Port (TM) Vascular Access System (Jun 9, 1988)
- K880297: Sea - Port Infusion Set (Feb 19, 1988)
- K874414: Hypodermic Needles, Single Lumen (Jan 14, 1988)

Source page: https://510kreport.com/company/harbor-medical-devices