FDA 510(k)

Clarity Reveal

K-Number: K171356 · 2017-08-03

Decision Date2017-08-03

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Clarity Reveal is the device name listed in this FDA 510(k) record. The listed applicant is Ceevra, Inc.. It received FDA 510(k) clearance on 2017-08-03 under 510(k) number K171356. 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 Clarity Reveal?

Clarity Reveal is a medical device that received FDA 510(k) clearance on 2017-08-03. The listed applicant is Ceevra, Inc.. The 510(k) number is K171356.

When did Clarity Reveal receive FDA 510(k) clearance?

Clarity Reveal received FDA 510(k) clearance on 2017-08-03, under 510(k) number K171356.

Who is the listed applicant for Clarity Reveal?

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

What is the FDA product code for Clarity Reveal?

The FDA product code for Clarity Reveal is LLZ.

Other records listing Ceevra, Inc. as applicant

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.

K243933Ceevra Reveal 3+K233568Ceevra Reveal 3+K222676Ceevra Reveal 3 K173274Ceevra Reveal 2.0

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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.