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Bio-Dyne, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900691BIODYNE INSTRUMENT WIPESMarch 8, 1990
K883984HEMORX COLD PACKDecember 22, 1988
K864261MODEL 3500 INFANT RESPIRATION & HEART RATE MONITORMarch 27, 1987