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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 the device name listed in this FDA 510(k) record. The listed applicant is Cgx, LLC. It received FDA 510(k) clearance on 2021-05-20 under 510(k) 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. The listed applicant is Cgx, LLC. The 510(k) number is K203331.

When did Quick-20m receive FDA 510(k) clearance?

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

Who is the listed applicant for Quick-20m?

The FDA 510(k) record lists Cgx, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: GWL)

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.

K243746Delphi AmplifierQuantalx NeroscienceK242832NExT Station; NExT Station AdvancedEb Neuro S.P.A.K242305BE Plus PRO, Neurotravel LIGHTEb Neuro S.P.A.K240646DreamClearSomnomed Technologies Inc., Doing Business AS RemwareK232210X-trodes System MX-TrodesK230148VlabDormotech Medical, Ltd.

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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