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FDA 510(k)

ANTI-WRINKLE (AGING) LIGHT, MODEL AAL

K-Number: K092800 · 2010-02-04

ApplicantLed Intellectual Properties, LLC
Decision Date2010-02-04
Product CodeONE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANTI-WRINKLE (AGING) LIGHT, MODEL AAL is the device name listed in this FDA 510(k) record. The listed applicant is Led Intellectual Properties, LLC. It received FDA 510(k) clearance on 2010-02-04 under 510(k) number K092800. The device is classified under product code ONE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-WRINKLE (AGING) LIGHT, MODEL AAL?

ANTI-WRINKLE (AGING) LIGHT, MODEL AAL is a medical device that received FDA 510(k) clearance on 2010-02-04. The listed applicant is Led Intellectual Properties, LLC. The 510(k) number is K092800.

When did ANTI-WRINKLE (AGING) LIGHT, MODEL AAL receive FDA 510(k) clearance?

ANTI-WRINKLE (AGING) LIGHT, MODEL AAL received FDA 510(k) clearance on 2010-02-04, under 510(k) number K092800.

Who is the listed applicant for ANTI-WRINKLE (AGING) LIGHT, MODEL AAL?

The FDA 510(k) record lists Led Intellectual Properties, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTI-WRINKLE (AGING) LIGHT, MODEL AAL?

The FDA product code for ANTI-WRINKLE (AGING) LIGHT, MODEL AAL is ONE.

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Other records listing Led Intellectual Properties, LLC 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.

K261482LightStim for Wrinkles (1984); LightStim for Acne (2038)K212771LightStim ElipsaK153399LightStim Professional LED BedK120775LIGHT FOR WRINKLESK101190LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTCK083580ANTI-WRINKLE LIGHT, MODEL 1302 AND PAIN THERAPY LIGHT, MODEL 1301

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Related Devices (Code: ONE)

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.

K250224handLITE (TN19S)iSMART Developments, Ltd.K171055Philips BlueControlPhilips Electronics Nederland B.V.K103415TANDA MAXPharos Life CorporationK100628PLASMALUXLSDaavlin Distributing Co.K091467BABY QUASARSilver Bay, LLCK091125CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2Verilux

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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