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FDA 510(k)

LIGHT RELIEF, MODEL LR150, LR200

K-Number: K070974 · 2007-05-24

ApplicantLight Relief, LLC
Decision Date2007-05-24
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGHT RELIEF, MODEL LR150, LR200 is the device name listed in this FDA 510(k) record. The listed applicant is Light Relief, LLC. It received FDA 510(k) clearance on 2007-05-24 under 510(k) number K070974. 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 LIGHT RELIEF, MODEL LR150, LR200?

LIGHT RELIEF, MODEL LR150, LR200 is a medical device that received FDA 510(k) clearance on 2007-05-24. The listed applicant is Light Relief, LLC. The 510(k) number is K070974.

When did LIGHT RELIEF, MODEL LR150, LR200 receive FDA 510(k) clearance?

LIGHT RELIEF, MODEL LR150, LR200 received FDA 510(k) clearance on 2007-05-24, under 510(k) number K070974.

Who is the listed applicant for LIGHT RELIEF, MODEL LR150, LR200?

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

What is the FDA product code for LIGHT RELIEF, MODEL LR150, LR200?

The FDA product code for LIGHT RELIEF, MODEL LR150, LR200 is ILY.

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Official Source

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