510(k) K053130 ยท DQA Oximeter
ONYX II FINGER PULSE OXIMETER, MODEL 9550
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 11, 2006 |
| Received | Nov 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053130
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.