K231385
- 510(k) number
- K231385
- Device name
- Rology Teleradiology Platform (v.1.22.1103)
- Applicant
- Rology, Inc. AR · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2023-09-20
- Date received
- 2023-05-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.4 MB · U.S. public domain
Also available from FDA: K231385.pdf
Official FDA record: K231385
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.