510(k) K953817 ยท DQA Oximeter
ARISTO MEDICAL MODEL 2101 PATIENT MONITOR
| Applicant | Aristo Medical Products, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Nov 22, 1995 |
| Received | Aug 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953817
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.