K240957
- 510(k) number
- K240957
- Device name
- Catapult Guide Sheath
- Applicant
- Contract Medical International, GmbH DE
- Product code
- DYB — Introducer, Catheter
- Decision date
- 2024-08-14
- Date received
- 2024-04-08
- 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: K240957.pdf
Official FDA record: K240957
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.