Class Class II

ScreenDx (K241891)

K241891 2025-01-10 Traditional
Home/ Devices/ ScreenDx (K241891)

Description

ScreenDx by Imvaria, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241891
Clearance Date2025-01-10
Clearance TypeTraditional
Product CodeQWO
Regulation Number892.2085

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top