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Helmer Labs, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K812533PLATELET AGITATORSeptember 29, 1981
K802608HEMATIC BLOOD MIXERDecember 11, 1980
K770830PLATELET AGITATORJuly 11, 1977