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FDA 510(k)

Mercu 1717V

K-Number: K222886 · 2022-10-20

Decision Date2022-10-20
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Mercu 1717V is a medical device manufactured by Iray Technology Taicang , Ltd.. It received FDA 510(k) clearance on 2022-10-20 under approval number K222886. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mercu 1717V?

Mercu 1717V is a medical device that received FDA 510(k) clearance on 2022-10-20. It is manufactured by Iray Technology Taicang , Ltd.. The 510(k) number is K222886.

When was Mercu 1717V approved by the FDA?

Mercu 1717V received FDA 510(k) clearance on 2022-10-20, under approval number K222886.

What company makes Mercu 1717V?

Mercu 1717V is manufactured by Iray Technology Taicang , Ltd..

What is the FDA product code for Mercu 1717V?

The FDA product code for Mercu 1717V is MQB.

Other Devices by Iray Technology Taicang , Ltd.

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Related Devices (Code: MQB)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.