510(k) K063661 ยท NLF Oximeter, Reprocessed
RENU REPROCESSED NELLCOR OXYSENSOR, MODELS D-20 AND I-20
| Applicant | Renu Medical, Inc., Everett WA, US |
| Decision | Substantially Equivalent, May 25, 2007 |
| Received | Dec 8, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063661
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.