510(k) K220647 ยท DQY Catheter, Percutaneous
GuideLiner Coast, 5.5F (5270); GuideLiner Coast, 6F (5271); GuideLiner Coast, 7F (5272); GuideLiner Coast, 8F (5273)
| Applicant | Vascular Solutions, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 18, 2022 |
| Received | Mar 7, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220647
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.