Medical Device Manufacturer · US , Indianapolis , IN

Flotec, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Flotec, Inc. Anesthesiology ✕

2 devices
1-2 of 2
Cleared Jul 10, 1997
FLOTEC OXYSAVRR (S)
K970371 · NFB
Anesthesiology · 160d
Cleared Apr 26, 1990
AMBU OXYGEN REGULATOR
K901623 · CAN
Anesthesiology · 20d
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