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FDA 510(k)

LIGHTSTREAM LOW LEVEL LASER

K-Number: K081166 · 2009-04-03

ApplicantSolica Corporation
Decision Date2009-04-03
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGHTSTREAM LOW LEVEL LASER is the device name listed in this FDA 510(k) record. The listed applicant is Solica Corporation. It received FDA 510(k) clearance on 2009-04-03 under 510(k) number K081166. 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 LIGHTSTREAM LOW LEVEL LASER?

LIGHTSTREAM LOW LEVEL LASER is a medical device that received FDA 510(k) clearance on 2009-04-03. The listed applicant is Solica Corporation. The 510(k) number is K081166.

When did LIGHTSTREAM LOW LEVEL LASER receive FDA 510(k) clearance?

LIGHTSTREAM LOW LEVEL LASER received FDA 510(k) clearance on 2009-04-03, under 510(k) number K081166.

Who is the listed applicant for LIGHTSTREAM LOW LEVEL LASER?

The FDA 510(k) record lists Solica Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHTSTREAM LOW LEVEL LASER?

The FDA product code for LIGHTSTREAM LOW LEVEL LASER 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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