510(k) K964055 ยท DQA Oximeter
FLEXI-SITE (E203-01)/ FLEXI-FIT (E300)
| Applicant | Epic Medical Equipment Services, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Feb 21, 1997 |
| Received | Oct 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964055
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.