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FDA 510(k)

Quick-20m

K-Number: K203331 · 2021-05-20

ApplicantCgx, LLC
Decision Date2021-05-20
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Quick-20m is a medical device manufactured by Cgx, LLC. It received FDA 510(k) clearance on 2021-05-20 under approval number K203331. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Quick-20m?

Quick-20m is a medical device that received FDA 510(k) clearance on 2021-05-20. It is manufactured by Cgx, LLC. The 510(k) number is K203331.

When was Quick-20m approved by the FDA?

Quick-20m received FDA 510(k) clearance on 2021-05-20, under approval number K203331.

What company makes Quick-20m?

Quick-20m is manufactured by Cgx, LLC.

What is the FDA product code for Quick-20m?

The FDA product code for Quick-20m is GWL.

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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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