510(k) K001930 ยท DQA Oximeter
MODEL 8500, HAND HELD PULSE OXIMETER, MODEL 8500
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 20, 2000 |
| Received | Jun 26, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001930
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.