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FDA 510(k)

LIGHTWAVE INFRARED LAMPS LW10D AND LW30D

K-Number: K024027 · 2003-12-03

ApplicantSkytech Enterprises, Inc.
Decision Date2003-12-03
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGHTWAVE INFRARED LAMPS LW10D AND LW30D is the device name listed in this FDA 510(k) record. The listed applicant is Skytech Enterprises, Inc.. It received FDA 510(k) clearance on 2003-12-03 under 510(k) number K024027. 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 LIGHTWAVE INFRARED LAMPS LW10D AND LW30D?

LIGHTWAVE INFRARED LAMPS LW10D AND LW30D is a medical device that received FDA 510(k) clearance on 2003-12-03. The listed applicant is Skytech Enterprises, Inc.. The 510(k) number is K024027.

When did LIGHTWAVE INFRARED LAMPS LW10D AND LW30D receive FDA 510(k) clearance?

LIGHTWAVE INFRARED LAMPS LW10D AND LW30D received FDA 510(k) clearance on 2003-12-03, under 510(k) number K024027.

Who is the listed applicant for LIGHTWAVE INFRARED LAMPS LW10D AND LW30D?

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

What is the FDA product code for LIGHTWAVE INFRARED LAMPS LW10D AND LW30D?

The FDA product code for LIGHTWAVE INFRARED LAMPS LW10D AND LW30D 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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