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Hypertec, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K002795 MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMSCBF2000-12-06 View
510(k) K002794 MODEL 5000 MULTIPLACE HYPERBARIC THERAPYCBF2000-12-06 View
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