510(k) K863857 ยท DQA Oximeter
PULSE-OX
| Applicant | Life Design Systems, Inc., Carrollton TX, US |
| Decision | Substantially Equivalent, Oct 7, 1987 |
| Received | Oct 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863857
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.