Harbor Medical Devices, Inc.
Harbor Medical Devices, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1989.
Top product codes for Harbor Medical Devices, Inc.
Recent clearances by Harbor Medical Devices, Inc.
- K884628 — HARBORIN CENTRAL VENOUS CATHETER
- K890518 — SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM
- K882657 — HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT
- K881884 — HARBOR CENTRAL VENOUS CATHETER
- K882190 — S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM
- K880297 — SEA - PORT INFUSION SET
- K874414 — HYPODERMIC NEEDLES, SINGLE LUMEN
Data sourced from openFDA. This site is unofficial and independent of the FDA.