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Amdia Medical Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K791338DUAL HEAD STETHOSCOPEAugust 10, 1979
K791334MULTISCOPEAugust 10, 1979
K791335NURSESCOPEAugust 10, 1979
K791333BOWLES STETHOSCOPEAugust 10, 1979
K791336BUCKS NEUROLOGICAL HAMMERAugust 3, 1979
K791337TAYLOR NEUROLOGICAL HAMMERAugust 3, 1979