510(k) K220363 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
VPS Rhythm DLX Device with TipTracker Technology
| Applicant | Arrow International, LLC (A subsidiary of Teleflex, Inc.), Morrisville NC, US |
| Decision | Substantially Equivalent, Aug 22, 2022 |
| Received | Feb 8, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220363
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.