510(k) K001121 ยท CBF Chamber, Hyperbaric
OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS)
| Applicant | Engineered Medical Technology, Inc., Victoria TX, US |
| Decision | Substantially Equivalent, Nov 29, 2001 |
| Received | Apr 7, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K001121
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.