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FDA 510(k)

DEL SOL RED LIGHT THERAPY SYSTEM

K-Number: K072399 · 2008-05-23

ApplicantEdge Systems, Inc.
Decision Date2008-05-23
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DEL SOL RED LIGHT THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Edge Systems, Inc.. It received FDA 510(k) clearance on 2008-05-23 under 510(k) number K072399. 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 DEL SOL RED LIGHT THERAPY SYSTEM?

DEL SOL RED LIGHT THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Edge Systems, Inc.. The 510(k) number is K072399.

When did DEL SOL RED LIGHT THERAPY SYSTEM receive FDA 510(k) clearance?

DEL SOL RED LIGHT THERAPY SYSTEM received FDA 510(k) clearance on 2008-05-23, under 510(k) number K072399.

Who is the listed applicant for DEL SOL RED LIGHT THERAPY SYSTEM?

The FDA 510(k) record lists Edge Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEL SOL RED LIGHT THERAPY SYSTEM?

The FDA product code for DEL SOL RED LIGHT THERAPY 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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