510(k) K092101 ยท DQA Oximeter
REUSABLE PULSE OXIMETER SENSOR, MODEL 8000 SERIES
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 21, 2009 |
| Received | Jul 14, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092101
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.