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Omp Laboratories, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K780703
CUFF PACER
July 17, 1978
K760402
SYRINGE SET, 3-WAY THERMODILUTIN
August 23, 1976