510(k) K181904 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
5 FR Dual Lumen Piper PICC
| Applicant | Piper Access, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 25, 2018 |
| Received | Jul 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181904
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.