510(k) K171483 ยท PND Midline Catheter
ArchFlo CT Midline
| Applicant | Medcomp (Dba Medical Components, Inc.), Harleysville PA, US |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | May 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171483
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.