Harmac Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Harmac Medical Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Harmac Medical Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Buffalo, US.
Historical record: 8 cleared submissions from 1995 to 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Harmac Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Harmac Medical Products, Inc.
8 devices
Cleared
Aug 29, 2002
HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001
General Hospital
79d
Cleared
Oct 16, 1997
HARMAC BALLOON ANGIOGRAPHIC CATHETER
Cardiovascular
475d
Cleared
Oct 16, 1997
HARMAC BALLOON WEDGE PRESSURE CATHETER
Cardiovascular
475d
Cleared
Oct 15, 1997
HARMAC TEMPORARY PACING CATHETER WITH BALLOON
Cardiovascular
474d
Cleared
Aug 14, 1997
HARMAC BIPOLAR TEMPORARY PACING CATHETER WITH STYLET
Cardiovascular
412d
Cleared
Aug 14, 1997
HARMAC THERMODILUTION CATHETER
Cardiovascular
412d
Cleared
Jun 25, 1997
HARMAC QUADPOLAR MAPPING PACING CATHETER
Cardiovascular
362d
Cleared
Sep 01, 1995
HARMAC EXTENSION INFUSION SET
General Hospital
186d