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Medishield, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K781103SPECTRASCANSeptember 27, 1978
K780645HMD-2000 BATTERY-POWERED MINI-DRILL, THEMay 3, 1978
K780646AIR-PWOERED COLDRILLApril 28, 1978
K780202MONOMER EVACUATION SYSTEMFebruary 21, 1978
K770161MICROFENESTRATED HIP REPLACEMENT COMPON.January 26, 1977
K761020ANKLE (FREEMAN-SWANSON)November 23, 1976
K761021ANKLE INSTRUMENTS (FREEMAN-SWANSON)November 23, 1976
K760668SELECTATEC SYSTEMSeptember 27, 1976