Meditech International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meditech International, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Meditech International, Inc. has 5 FDA 510(k) cleared medical devices. Based in Stamford, US.
Historical record: 5 cleared submissions from 2003 to 2008. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Meditech International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meditech International, Inc.
5 devices
Cleared
Dec 18, 2008
BIOFLEX LD-R100 TREATMENT HEAD
Physical Medicine
218d
Cleared
Apr 02, 2008
LD-I 75 AND LD-I 200
Physical Medicine
205d
Cleared
Mar 13, 2006
BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS
Physical Medicine
245d
Cleared
Feb 24, 2005
BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS
Physical Medicine
227d
Cleared
Apr 10, 2003
BIOFLEX PROFESSIONAL THERAPY SYSTEM
Physical Medicine
163d