K253861
- 510(k) number
- K253861
- Device name
- ACORYS MAPPING SYSTEM
- Applicant
- Corify Care S.L ES
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2026-04-13
- Date received
- 2025-12-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K253861.pdf
Official FDA record: K253861
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.