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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Laminate Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-16 under 510(k) 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. The listed applicant is Laminate Medical Technologies , Ltd.. The 510(k) number is K240119.

When did VasQ receive FDA 510(k) clearance?

VasQ received FDA 510(k) clearance on 2024-02-16, under 510(k) number K240119.

Who is the listed applicant for VasQ?

The FDA 510(k) record lists Laminate Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VasQ?

The FDA product code for VasQ is QVQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT03242343VasQ External Support for Arteriovenous FistulaCOMPLETEDNCT06516653Post Market Study for VasQ, an External Support Implant for Arteriovenous FistulaRECRUITING

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.

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