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Medcraft Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K860467ELECTROSHOCK UNIT NEUROLOGY MODEL B-25November 10, 1986
K791795COMP-ACT IVSeptember 27, 1979
K760510MONITORING SYSTEM, REHABILITATIONAugust 30, 1976
K760509TREADMILL, DIAGNOSTICAugust 30, 1976
K760508ACCUTAPE 24August 30, 1976