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Flotec, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K970371
FLOTEC OXYSAVRR (S)
July 10, 1997
K901623
AMBU OXYGEN REGULATOR
April 26, 1990