510(k) K111773 ยท NLF Oximeter, Reprocessed
RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
| Applicant | Renu Medical, Inc., Everett WA, US |
| Decision | Substantially Equivalent, Nov 16, 2011 |
| Received | Jun 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111773
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.