K243435
- 510(k) number
- K243435
- Device name
- Magnetic Localization Patch Kit (AFR-00021)
- Applicant
- Medtronic, Inc. MN · US
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2024-12-05
- Date received
- 2024-11-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243435.pdf
Official FDA record: K243435
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.