Medicon, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Medicon, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1981 to 1997.
Browse the FDA 510(k) cleared devices submitted by Medicon, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Apr 23, 1997
SERVOTRONIC EC100 SYSTEM
Orthopedic
330d
Cleared
Jun 22, 1995
TITANIUM MANDIBULAR FRACTURE SYSTEM
Dental
45d
Cleared
Jan 09, 1986
TENS GB1001 DEVICE
Neurology
314d
Cleared
Aug 21, 1985
INFRARAX DEVICE
Physical Medicine
173d
Cleared
Apr 01, 1985
GAUZE ASORBABLE
General & Plastic Surgery
119d
Cleared
Mar 05, 1985
ABSORBABLE GAUZE PRODUCTS
General & Plastic Surgery
102d
Cleared
Feb 21, 1985
WHEELCHAIRS
Physical Medicine
90d
Cleared
Jan 10, 1985
GOWNS, SURGICAL
General Hospital
38d
Cleared
Jan 10, 1985
CAPS (O.R. NURSE, SURGICAL)
General & Plastic Surgery
38d
Cleared
Jan 10, 1985
SHOE COVERS
General Hospital
38d
Cleared
Feb 27, 1984
VACUUM STRETCHER IMMOBILIZER
General Hospital
53d
Cleared
Dec 30, 1982
MODEL 8300 TESTER
Cardiovascular
65d