Class Class II

Vivatmo pro-S (K243926)

K243926 2025-09-11 Traditional
Home/ Devices/ Vivatmo pro-S (K243926)

Description

Vivatmo pro-S by Bosch Healthcare Solutions GmbH — FDA 510(k) cleared clinical toxicology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243926
Clearance Date2025-09-11
Clearance TypeTraditional
Product CodeMXA
Regulation Number862.3080

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top