510(k) K131023 ยท NFB Conserver, Oxygen
THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN
| Applicant | Medical Products, LLC, Indianapolis IN, US |
| Decision | Substantially Equivalent, Oct 11, 2013 |
| Received | Apr 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131023
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.