Medcraft Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medcraft Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medcraft Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1976 to 1986. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medcraft Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medcraft Corp.
5 devices
Cleared
Nov 10, 1986
ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
Neurology
277d
Cleared
Sep 27, 1979
COMP-ACT IV
Cardiovascular
13d
Cleared
Aug 30, 1976
ACCUTAPE 24
Cardiovascular
6d
Cleared
Aug 30, 1976
TREADMILL, DIAGNOSTIC
Physical Medicine
6d
Cleared
Aug 30, 1976
MONITORING SYSTEM, REHABILITATION
Cardiovascular
6d