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The Timeter Group

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K871452CLASSIC (TM) 200 OXYGEN FLOWMETERJune 22, 1987
K862171MP-500 ELECTRONIC NEBULIZERJuly 14, 1986
K852374OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18July 12, 1985
K844556KHM 2000 DRIP WATCHERJanuary 14, 1985