FDA 510(k)

Qmenta Care Platform Family

K-Number: K202718 · 2021-06-16

Decision Date2021-06-16

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Qmenta Care Platform Family is the device name listed in this FDA 510(k) record. The listed applicant is Mint Labs, Inc., D/B/A. Qmenta. It received FDA 510(k) clearance on 2021-06-16 under 510(k) number K202718. 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 Qmenta Care Platform Family?

Qmenta Care Platform Family is a medical device that received FDA 510(k) clearance on 2021-06-16. The listed applicant is Mint Labs, Inc., D/B/A. Qmenta. The 510(k) number is K202718.

When did Qmenta Care Platform Family receive FDA 510(k) clearance?

Qmenta Care Platform Family received FDA 510(k) clearance on 2021-06-16, under 510(k) number K202718.

Who is the listed applicant for Qmenta Care Platform Family?

The FDA 510(k) record lists Mint Labs, Inc., D/B/A. Qmenta as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Qmenta Care Platform Family?

The FDA product code for Qmenta Care Platform Family is LLZ.

Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.