510(k) K132567 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER SINGLE LUMEN, ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER DUAL LUMEN
| Applicant | Covidien, Mansfield MA, US |
| Decision | Substantially Equivalent, Nov 5, 2013 |
| Received | Aug 15, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132567
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.