Medical Device Manufacturer · US , Deer Field , IL

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

2 submissions · 2 cleared · Since 2000

Recent clearances: MODEL 5000 MULTIPLACE HYPERBARIC THERAPY, MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS

View 2 510(k) Devices ↓

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

Anesthesiology · 90d

Cleared Dec 06, 2000

MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS

Anesthesiology · 90d