K241372
- 510(k) number
- K241372
- Device name
- Advisor HD Grid X Mapping Catheter, Sensor Enabled
- Applicant
- ABBOTT MEDICAL MN · US
- Product code
- MTD — Catheter, Intracardiac Mapping, High-Density Array
- Decision date
- 2024-07-09
- Date received
- 2024-05-15
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K241372.pdf
Official FDA record: K241372
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.