FDA 510(k) Applications Submitted by HYPERTEC, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K002794 | 09/07/2000 | MODEL 5000 MULTIPLACE HYPERBARIC THERAPY | HYPERTEC, INC. |
| K002795 | 09/07/2000 | MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS | HYPERTEC, INC. |
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