510(k) K920966 ยท DQA Oximeter
SDI OXYGEN/DIGITAL OXYGEN TRANSDUCERS (DOT)
| Applicant | Aristo Medical Products, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Jul 16, 1993 |
| Received | Mar 2, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920966
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.