K252227
- 510(k) number
- K252227
- Device name
- Pounce(TM) Sheath
- Applicant
- Surmodics,Inc. MN · US
- Product code
- DYB — Introducer, Catheter
- Decision date
- 2025-09-24
- Date received
- 2025-07-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K252227.pdf
Official FDA record: K252227
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.