K242129
- 510(k) number
- K242129
- Device name
- VitalRhythm
- Applicant
- Vitalconnect, Inc. CA · US
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2025-04-17
- Date received
- 2024-07-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242129.pdf
Official FDA record: K242129
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.