510(k) K102560 ยท NLF Oximeter, Reprocessed
REPROCESSED PULSE OXIMETER SENSORS
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Feb 18, 2011 |
| Received | Sep 7, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102560
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.