vPATCH
K-Number: K223595 · 2023-05-01
ApplicantVirility Medical , Ltd.
Decision Date2023-05-01
Product CodeQRC
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
vPATCH is a medical device manufactured by Virility Medical , Ltd.. It received FDA 510(k) clearance on 2023-05-01 under approval number K223595. The device is classified under product code QRC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the vPATCH?
vPATCH is a medical device that received FDA 510(k) clearance on 2023-05-01. It is manufactured by Virility Medical , Ltd.. The 510(k) number is K223595.
When was vPATCH approved by the FDA?
vPATCH received FDA 510(k) clearance on 2023-05-01, under approval number K223595.
What company makes vPATCH?
vPATCH is manufactured by Virility Medical , Ltd..
What is the FDA product code for vPATCH?
The FDA product code for vPATCH is QRC.
Other Devices by Virility Medical , Ltd.
Related Devices (Code: QRC)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.