K231160
- 510(k) number
- K231160
- Device name
- Cardio Q50, Cardio Q70
- Applicant
- Bionet Co., Ltd. KR
- Product code
- DPS — Electrocardiograph
- Decision date
- 2023-12-15
- Date received
- 2023-04-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231160.pdf
Official FDA record: K231160
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.