Holgrath Medical Technologies, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Holgrath Medical Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Cheshire, US.
Historical record: 6 cleared submissions from 1995 to 1996. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Holgrath Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 31, 1996
HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET
Anesthesiology
103d
Cleared
Jul 25, 1995
HOLGRATH METAL-HUB, EPIDURAL NEEDLE
Anesthesiology
225d
Cleared
Jun 07, 1995
HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE
Anesthesiology
245d
Cleared
Jun 07, 1995
HOLGRATH PLASTIC-HUB EPIDURAL NEEDLE
Anesthesiology
245d
Cleared
Jun 07, 1995
HOLGRATH PLASTIC-HUB, QUINCKE SPINAL NEEDLE
Anesthesiology
245d
Cleared
Jun 07, 1995
HOLGRATH PLASTIC-HUB, COICAL POINT SPINAL NEEDLE
Anesthesiology
245d