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FDA 510(k)

XD

K-Number: K220779 · 2022-04-15

ApplicantMirada Medical, Ltd.
Decision Date2022-04-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XD is a medical device manufactured by Mirada Medical, Ltd.. It received FDA 510(k) clearance on 2022-04-15 under approval number K220779. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XD?

XD is a medical device that received FDA 510(k) clearance on 2022-04-15. It is manufactured by Mirada Medical, Ltd.. The 510(k) number is K220779.

When was XD approved by the FDA?

XD received FDA 510(k) clearance on 2022-04-15, under approval number K220779.

What company makes XD?

XD is manufactured by Mirada Medical, Ltd..

What is the FDA product code for XD?

The FDA product code for XD is LLZ.

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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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