510(k) K181738 ยท DQA Oximeter
Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors
| Applicant | Surgical Instrument Service and Savings Inc (Dba Medline, Redmond OR, US |
| Decision | Substantially Equivalent, Mar 22, 2019 |
| Received | Jul 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181738
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.