Class Class II

syngo.via MI Workflows; Scenium; syngo MBF (K242275)

K242275 2024-08-30 Special
Home/ Devices/ syngo.via MI Workflows; Scenium;…

Description

syngo.via MI Workflows; Scenium; syngo MBF by Siemens Medical Solutions USA, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242275
Clearance Date2024-08-30
Clearance TypeSpecial
Product CodeQIH
Regulation Number892.2050

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top