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Foregger
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K771057
ANESTHESIA MACHINE
July 5, 1977
K760263
I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)
August 4, 1976