FDA 510(k)

Cuptimize

K-Number: K203651 · 2021-02-26

Decision Date2021-02-26

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Cuptimize is the device name listed in this FDA 510(k) record. The listed applicant is Cuptimize, Inc.. It received FDA 510(k) clearance on 2021-02-26 under 510(k) 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. The listed applicant is Cuptimize, Inc.. The 510(k) number is K203651.

When did Cuptimize receive FDA 510(k) clearance?

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

Who is the listed applicant for Cuptimize?

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

What is the FDA product code for Cuptimize?

The FDA product code for Cuptimize 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.

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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.