Medical Device Manufacturer · US , Boston , MA

Harbor Medical Devices, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1988

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Harbor Medical Devices, Inc. General Hospital ✕

4 devices

1-4 of 4

Cleared Apr 21, 1989

SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM

General Hospital · 78d

Cleared Jun 09, 1988

S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM

General Hospital · 16d

Cleared Feb 19, 1988

SEA - PORT INFUSION SET

General Hospital · 25d

Cleared Jan 14, 1988

HYPODERMIC NEEDLES, SINGLE LUMEN

General Hospital · 78d