K243691
- 510(k) number
- K243691
- Device name
- LiquID .051 LP Guide Catheter Extension
- Applicant
- Seigla Medical, Inc. MN · US
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2025-04-04
- Date received
- 2024-11-26
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K243691.pdf
Official FDA record: K243691
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.