Harbor Medical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Harbor Medical Devices, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Harbor Medical Devices, Inc. has 7 FDA 510(k) cleared medical devices. Based in Boston, US.
Historical record: 7 cleared submissions from 1988 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Harbor Medical Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Harbor Medical Devices, Inc.
7 devices
Cleared
May 15, 1989
HARBORIN CENTRAL VENOUS CATHETER
Cardiovascular
189d
Cleared
Apr 21, 1989
SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM
General Hospital
78d
Cleared
Dec 13, 1988
HARBOR S.E.A.-PORT SURGICAL ACCESSORY KIT
Cardiovascular
167d
Cleared
Jul 28, 1988
HARBOR CENTRAL VENOUS CATHETER
Cardiovascular
85d
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