510(k) K041127 ยท NLF Oximeter, Reprocessed
MODIFICATION TO: REPROCESSED OXIMAX PULSE OXIMETER SENSORS
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Sep 23, 2004 |
| Received | Apr 30, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041127
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.