Class Class II

vPATCH (K223595)

K223595 2023-05-01 Traditional
Home/ Devices/ vPATCH (K223595)

Description

vPATCH by Virility Medical , Ltd. — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223595
Clearance Date2023-05-01
Clearance TypeTraditional
Product CodeQRC
Regulation Number876.5026

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top