510(k) K002795 ยท CBF Chamber, Hyperbaric
MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS
| Applicant | Hypertec, Inc., Deer Field IL, US |
| Decision | Substantially Equivalent, Dec 6, 2000 |
| Received | Sep 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002795
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.