510(k) K051759 ยท CBF Chamber, Hyperbaric
FLEXI-LITE, MODEL FL-V1.2
| Applicant | Performance Hyperbarics, Makawao HI, US |
| Decision | Substantially Equivalent, Nov 17, 2005 |
| Received | Jun 29, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051759
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.