510(k) K012600 ยท NLF Oximeter, Reprocessed
CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25L
| Applicant | Clearmedical, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Jul 3, 2002 |
| Received | Aug 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012600
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.