Medical Device Manufacturer · US , Deer Field , IL

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

2 submissions · 2 cleared · Since 2000
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hypertec, Inc. Anesthesiology ✕
2 devices
1-2 of 2
Cleared Dec 06, 2000
MODEL 5000 MULTIPLACE HYPERBARIC THERAPY
K002794 · CBF
Anesthesiology · 90d
Cleared Dec 06, 2000
MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS
K002795 · CBF
Anesthesiology · 90d
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