510(k) K072194 ยท NLF Oximeter, Reprocessed
RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25
| Applicant | Renu Medical, Inc., Everett WA, US |
| Decision | Substantially Equivalent, Nov 29, 2007 |
| Received | Aug 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072194
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.