K241538
- 510(k) number
- K241538
- Device name
- TriClip Steerable Guide Catheter
- Applicant
- ABBOTT MEDICAL MN · US
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2024-08-26
- Date received
- 2024-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K241538.pdf
Official FDA record: K241538
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.