LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC
K-Number: K101190 · 2010-07-01
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Device Summary
Frequently Asked Questions
What is the LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC?
LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC is a medical device that received FDA 510(k) clearance on 2010-07-01. The listed applicant is Led Intellectual Properties, LLC. The 510(k) number is K101190.
When did LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC receive FDA 510(k) clearance?
LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC received FDA 510(k) clearance on 2010-07-01, under 510(k) number K101190.
Who is the listed applicant for LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC?
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 LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC?
The FDA product code for LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC is OHS.
Related Clinical Trials
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.
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.
Related Devices (Code: OHS)
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.
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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