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FDA 510(k)

HAIRMAX LASERCOMB

K-Number: K093499 · 2009-11-23

Decision Date2009-11-23
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAIRMAX LASERCOMB is the device name listed in this FDA 510(k) record. The listed applicant is Lexington International, LLC. It received FDA 510(k) clearance on 2009-11-23 under 510(k) number K093499. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAIRMAX LASERCOMB?

HAIRMAX LASERCOMB is a medical device that received FDA 510(k) clearance on 2009-11-23. The listed applicant is Lexington International, LLC. The 510(k) number is K093499.

When did HAIRMAX LASERCOMB receive FDA 510(k) clearance?

HAIRMAX LASERCOMB received FDA 510(k) clearance on 2009-11-23, under 510(k) number K093499.

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.

View all 7 devices →

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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