Dan Med, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dan Med, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Dan Med, Inc. has 6 FDA 510(k) cleared medical devices. Based in Denver, US.
Historical record: 6 cleared submissions from 1997 to 2002. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Dan Med, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dan Med, Inc.
6 devices
Cleared
Apr 04, 2002
TRUWAVE
Neurology
190d
Cleared
Nov 08, 2001
NEUROMOVE NM900
Physical Medicine
72d
Cleared
Jun 27, 2001
EMS 3000
Physical Medicine
106d
Cleared
Nov 02, 1999
IF8000
Physical Medicine
204d
Cleared
Nov 10, 1997
AM800 AUTOMOVE EMG TRIGGERED ELECTRICAL MUSCLE STIMULATION
Physical Medicine
90d
Cleared
Aug 14, 1997
ELPHA 2000 CONTI
Gastroenterology & Urology
274d