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FDA 510(k)

Clarity Reveal

K-Number: K171356 · 2017-08-03

ApplicantCeevra, Inc.
Decision Date2017-08-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Clarity Reveal is a medical device manufactured by Ceevra, Inc.. It received FDA 510(k) clearance on 2017-08-03 under approval 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. It is manufactured by Ceevra, Inc.. The 510(k) number is K171356.

When was Clarity Reveal approved by the FDA?

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

What company makes Clarity Reveal?

Clarity Reveal is manufactured by Ceevra, Inc..

What is the FDA product code for Clarity Reveal?

The FDA product code for Clarity Reveal is LLZ.

Other Devices by Ceevra, Inc.

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

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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