510(k) K962871 ยท CBF Chamber, Hyperbaric
ODS1 - HOOD DRIVER
| Applicant | Reimers Systems, Inc., Springfield VA, US |
| Decision | Substantially Equivalent, Oct 23, 1996 |
| Received | Jul 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962871
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.