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FDA 510(k)

Qmenta Care Platform Family

K-Number: K202718 · 2021-06-16

ApplicantMint Labs, Inc., D/B/A. Qmenta
Decision Date2021-06-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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

When was Qmenta Care Platform Family approved by the FDA?

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

What company makes Qmenta Care Platform Family?

Qmenta Care Platform Family is manufactured by Mint Labs, Inc., D/B/A. Qmenta.

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

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

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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.

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