Class Class II

Veloxion System (K230205)

K230205 2023-02-24 Special
Home/ Devices/ Veloxion System (K230205)

Description

Veloxion System by Corinth Medtech, Inc. — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230205
Clearance Date2023-02-24
Clearance TypeSpecial
Product CodeFJL
Regulation Number876.1500

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