HAIRMAX LASERCOMB
K-Number: K103368 · 2011-04-06
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Device Summary
Frequently Asked Questions
What is the HAIRMAX LASERCOMB?
HAIRMAX LASERCOMB is a medical device that received FDA 510(k) clearance on 2011-04-06. The listed applicant is Lexington International, LLC. The 510(k) number is K103368.
When did HAIRMAX LASERCOMB receive FDA 510(k) clearance?
HAIRMAX LASERCOMB received FDA 510(k) clearance on 2011-04-06, under 510(k) number K103368.
Who is the listed applicant for HAIRMAX LASERCOMB?
The FDA 510(k) record lists Lexington International, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAIRMAX LASERCOMB?
The FDA product code for HAIRMAX LASERCOMB is OAP.
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 Lexington International, 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: OAP)
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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