Medical Device Manufacturer · US , Claremont , NH

Plastiflex Group NV - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Plastiflex Group NV Anesthesiology ✕
2 devices
1-2 of 2
Cleared Mar 24, 2016
Hybernite RT
K151461 · BZE
Anesthesiology · 297d
Cleared Apr 14, 2010
HYBERNITE RAINOUT CONTROL SYSTEM
K100104 · BZE
Anesthesiology · 91d
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