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FDA 510(k)

CLEARFLASH AC2100 COSMETIC SYSTEM

K-Number: K111937 · 2012-02-08

ApplicantClearflash Technologies, Inc.
Decision Date2012-02-08
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEARFLASH AC2100 COSMETIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Clearflash Technologies, Inc.. It received FDA 510(k) clearance on 2012-02-08 under 510(k) number K111937. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARFLASH AC2100 COSMETIC SYSTEM?

CLEARFLASH AC2100 COSMETIC SYSTEM is a medical device that received FDA 510(k) clearance on 2012-02-08. The listed applicant is Clearflash Technologies, Inc.. The 510(k) number is K111937.

When did CLEARFLASH AC2100 COSMETIC SYSTEM receive FDA 510(k) clearance?

CLEARFLASH AC2100 COSMETIC SYSTEM received FDA 510(k) clearance on 2012-02-08, under 510(k) number K111937.

Who is the listed applicant for CLEARFLASH AC2100 COSMETIC SYSTEM?

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

What is the FDA product code for CLEARFLASH AC2100 COSMETIC SYSTEM?

The FDA product code for CLEARFLASH AC2100 COSMETIC SYSTEM is OLP.

Related Clinical Trials

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Related Devices (Code: OLP)

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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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