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Devices · VideaHealth, Inc

Videa Caries Assist

510(k)K213795RadiologyMYN

VideaHealth, Inc is listed for Videa Caries Assist (K213795). The FDA list gives April 21, 2022 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code MYN as “Analyzer, Medical Image”: For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K213795

Official FDA database record

Date of final decision
April 21, 2022
Company on the FDA list
VideaHealth, Inc
Lead panel
Radiology
Primary product code
MYN
openFDA device name for the code
Analyzer, Medical Image
Device class
2
Regulation number
892.2070
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers