510(k) K162377 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
PowerGlide Pro Midline Catheter
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Sep 22, 2016 |
| Received | Aug 24, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162377
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.