510(k) K220691 ยท DQY Catheter, Percutaneous
LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension
| Applicant | Seigla Medical, Inc., Buffalo MN, US |
| Decision | Substantially Equivalent, May 5, 2022 |
| Received | Mar 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220691
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.