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FDA 510(k)

BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM

K-Number: K052307 · 2005-12-16

ApplicantBeamline Corporation
Decision Date2005-12-16
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Beamline Corporation. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K052307. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM?

BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Beamline Corporation. The 510(k) number is K052307.

When did BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM receive FDA 510(k) clearance?

BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052307.

Who is the listed applicant for BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM?

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

What is the FDA product code for BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM?

The FDA product code for BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM is ILY.

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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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