510(k) K081927 ยท NLF Oximeter, Reprocessed
RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEO
| Applicant | Renu Medical, Inc., Everett WA, US |
| Decision | Substantially Equivalent, Feb 6, 2009 |
| Received | Jul 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081927
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.