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Pulmonox Medical Corp.

FDA Regulatory Profile

Pulmonox Medical Corp. 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 January 26, 2004.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K033779VIANOX DELIVERY SYSTEM, MODEL IIJanuary 26, 2004
K023014VIANOX DELIVERY SYSTEM, MODEL IAugust 14, 2003
K000653AERONOX UNIVERSAL, MODEL P/N 360000, AERONOX BEDSIDE, MODEL P/N 360001, AERONOX TRANSPORT TRANSPORT,August 4, 2000

FDA data resources