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FDA 510(k)

MB SYSTEM, BIOENERGY LIGHT THERAPY

K-Number: K030275 · 2004-11-29

ApplicantAmest Corp.
Decision Date2004-11-29
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MB SYSTEM, BIOENERGY LIGHT THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Amest Corp.. It received FDA 510(k) clearance on 2004-11-29 under 510(k) number K030275. 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 MB SYSTEM, BIOENERGY LIGHT THERAPY?

MB SYSTEM, BIOENERGY LIGHT THERAPY is a medical device that received FDA 510(k) clearance on 2004-11-29. The listed applicant is Amest Corp.. The 510(k) number is K030275.

When did MB SYSTEM, BIOENERGY LIGHT THERAPY receive FDA 510(k) clearance?

MB SYSTEM, BIOENERGY LIGHT THERAPY received FDA 510(k) clearance on 2004-11-29, under 510(k) number K030275.

Who is the listed applicant for MB SYSTEM, BIOENERGY LIGHT THERAPY?

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

What is the FDA product code for MB SYSTEM, BIOENERGY LIGHT THERAPY?

The FDA product code for MB SYSTEM, BIOENERGY LIGHT THERAPY 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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