Class Class II

VasoGuard (V10, V8, V6, V4, V2) (K233976)

K233976 2024-07-19 Traditional
Home/ Devices/ VasoGuard (V10, V8, V6,…

Description

VasoGuard (V10, V8, V6, V4, V2) by Corvascular Diagnostics, LLC — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233976
Clearance Date2024-07-19
Clearance TypeTraditional
Product CodeJOP
Regulation Number870.2880

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top