K252859
- 510(k) number
- K252859
- Device name
- ZEUS Platform (FG0501US)
- Applicant
- iRhythm Technologies, Inc. CA · US
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2026-05-29
- Date received
- 2025-09-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K252859.pdf
Official FDA record: K252859
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.