Hypertec, Inc.
MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS
SKU K002795UPC CBF
In Stock
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IIFDA 510(k) Cleared (K002795)
1
Free shipping on orders over $99 · 30-day returns
Hypertec, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS is an FDA 510(k)-cleared medical device (K002795) manufactured by Hypertec, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 5, 2000. Regulation: 8.
