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FDA 510(k)

COLD LIGHT SOURCE LOS 150

K-Number: K951829 · 1995-07-10

Decision Date1995-07-10
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

COLD LIGHT SOURCE LOS 150 is the device name listed in this FDA 510(k) record. The listed applicant is Laser-Optik-Systeme GmbH & Co. KG. It received FDA 510(k) clearance on 1995-07-10 under 510(k) number K951829. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLD LIGHT SOURCE LOS 150?

COLD LIGHT SOURCE LOS 150 is a medical device that received FDA 510(k) clearance on 1995-07-10. The listed applicant is Laser-Optik-Systeme GmbH & Co. KG. The 510(k) number is K951829.

When did COLD LIGHT SOURCE LOS 150 receive FDA 510(k) clearance?

COLD LIGHT SOURCE LOS 150 received FDA 510(k) clearance on 1995-07-10, under 510(k) number K951829.

Who is the listed applicant for COLD LIGHT SOURCE LOS 150?

The FDA 510(k) record lists Laser-Optik-Systeme GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLD LIGHT SOURCE LOS 150?

The FDA product code for COLD LIGHT SOURCE LOS 150 is EQH.

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 Laser-Optik-Systeme GmbH & Co. KG 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: EQH)

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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