510(k) K900843 ยท DQA Oximeter
OXIMAX 100
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Mar 28, 1990 |
| Received | Feb 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900843
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.