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Foregger

FDA Regulatory Profile

Foregger appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 5, 1977.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K771057ANESTHESIA MACHINEJuly 5, 1977
K760263I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)August 4, 1976

FDA data resources