510(k) K220331 ยท DQY Catheter, Percutaneous
091 Balloon Guide Catheter
| Applicant | Inneuroco, Inc., Pembroke Pines FL, US |
| Decision | Substantially Equivalent, Jul 29, 2022 |
| Received | Feb 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220331
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.