K253562
- 510(k) number
- K253562
- Device name
- medilogFD
- Applicant
- Schiller AG CH
- Product code
- MWJ — Electrocardiograph, Ambulatory (Without Analysis)
- Decision date
- 2026-08-14
- Date received
- 2025-11-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253562.pdf
Official FDA record: K253562
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.