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FDA 510(k)

Cuptimize

K-Number: K203651 · 2021-02-26

ApplicantCuptimize, Inc.
Decision Date2021-02-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Cuptimize is a medical device manufactured by Cuptimize, Inc.. It received FDA 510(k) clearance on 2021-02-26 under approval number K203651. 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 Cuptimize?

Cuptimize is a medical device that received FDA 510(k) clearance on 2021-02-26. It is manufactured by Cuptimize, Inc.. The 510(k) number is K203651.

When was Cuptimize approved by the FDA?

Cuptimize received FDA 510(k) clearance on 2021-02-26, under approval number K203651.

What company makes Cuptimize?

Cuptimize is manufactured by Cuptimize, Inc..

What is the FDA product code for Cuptimize?

The FDA product code for Cuptimize 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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