K240890
- 510(k) number
- K240890
- Device name
- PanopticAI Vital Signs
- Applicant
- PanopticAI technologies Limited HK
- Product code
- QME — Software For Optical Camera-Based Measurement Of Pul
- Decision date
- 2024-12-23
- Date received
- 2024-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K240890.pdf
Official FDA record: K240890
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.