K253232
- 510(k) number
- K253232
- Device name
- Seguin Annuloplasty Ring
- Applicant
- ABBOTT MEDICAL MN · US
- Product code
- KRH — Ring, Annuloplasty
- Decision date
- 2025-10-29
- Date received
- 2025-09-29
- 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: K253232.pdf
Official FDA record: K253232
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.