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FDA 510(k)

Monet Curing Laser

K-Number: K201904 · 2020-11-24

ApplicantCAO Group, Inc.
Decision Date2020-11-24
Product CodeQNF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Monet Curing Laser is the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2020-11-24 under 510(k) number K201904. The device is classified under product code QNF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Monet Curing Laser?

Monet Curing Laser is a medical device that received FDA 510(k) clearance on 2020-11-24. The listed applicant is CAO Group, Inc.. The 510(k) number is K201904.

When did Monet Curing Laser receive FDA 510(k) clearance?

Monet Curing Laser received FDA 510(k) clearance on 2020-11-24, under 510(k) number K201904.

Who is the listed applicant for Monet Curing Laser?

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

What is the FDA product code for Monet Curing Laser?

The FDA product code for Monet Curing Laser is QNF.

Other records listing CAO Group, Inc. as applicant

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Related Devices (Code: QNF)

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.

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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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