510(k) K810363 ยท DPZ Oximeter, Ear
EAR OXIMETER
| Applicant | Bio-Tek Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 27, 1981 |
| Received | Feb 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810363
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.