Dufco Electronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dufco Electronics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Dufco Electronics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Cambria, US.
Historical record: 4 cleared submissions from 1988 to 1988. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Dufco Electronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dufco Electronics, Inc.
4 devices
Cleared
Jul 18, 1988
MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.
Physical Medicine
102d
Cleared
Jul 18, 1988
UNIMODE(TM) POWER MODULE SYSTEM
Physical Medicine
102d
Cleared
Jul 18, 1988
MULTIMODE(TM) POWER MODULE SYSTEM
Physical Medicine
102d
Cleared
Jul 18, 1988
MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNING
Physical Medicine
102d