510(k) K243691 ยท DQY Catheter, Percutaneous
LiquID .051 LP Guide Catheter Extension
| Applicant | Seigla Medical, Inc., Buffalo MN, US |
| Decision | Substantially Equivalent, Apr 4, 2025 |
| Received | Nov 26, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243691
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.