VasQ
K-Number: K240119 · 2024-02-16
ApplicantLaminate Medical Technologies , Ltd.
Decision Date2024-02-16
Product CodeQVQ
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
VasQ is a medical device manufactured by Laminate Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-16 under approval number K240119. The device is classified under product code QVQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VasQ?
VasQ is a medical device that received FDA 510(k) clearance on 2024-02-16. It is manufactured by Laminate Medical Technologies , Ltd.. The 510(k) number is K240119.
When was VasQ approved by the FDA?
VasQ received FDA 510(k) clearance on 2024-02-16, under approval number K240119.
What company makes VasQ?
VasQ is manufactured by Laminate Medical Technologies , Ltd..
What is the FDA product code for VasQ?
The FDA product code for VasQ is QVQ.
Other Devices by Laminate Medical Technologies , Ltd.
Related Devices (Code: QVQ)
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.