Bio-Dyne, Inc.

FDA Regulatory Profile

Bio-Dyne, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 8, 1990.

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