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FDA 510(k)

LAZRPULSR 4X

K-Number: K041565 · 2005-03-03

ApplicantLed Healing Light, LLC
Decision Date2005-03-03
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LAZRPULSR 4X is the device name listed in this FDA 510(k) record. The listed applicant is Led Healing Light, LLC. It received FDA 510(k) clearance on 2005-03-03 under 510(k) number K041565. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAZRPULSR 4X?

LAZRPULSR 4X is a medical device that received FDA 510(k) clearance on 2005-03-03. The listed applicant is Led Healing Light, LLC. The 510(k) number is K041565.

When did LAZRPULSR 4X receive FDA 510(k) clearance?

LAZRPULSR 4X received FDA 510(k) clearance on 2005-03-03, under 510(k) number K041565.

Who is the listed applicant for LAZRPULSR 4X?

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

What is the FDA product code for LAZRPULSR 4X?

The FDA product code for LAZRPULSR 4X is NHN.

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Related Devices (Code: NHN)

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.

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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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