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FDA 510(k)

TLC MODELS ULK-H AND ULT-H INFRARED LAMPS

K-Number: K033035 · 2003-11-20

ApplicantTlc Marketing, Inc.
Decision Date2003-11-20
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TLC MODELS ULK-H AND ULT-H INFRARED LAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Tlc Marketing, Inc.. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K033035. 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 TLC MODELS ULK-H AND ULT-H INFRARED LAMPS?

TLC MODELS ULK-H AND ULT-H INFRARED LAMPS is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Tlc Marketing, Inc.. The 510(k) number is K033035.

When did TLC MODELS ULK-H AND ULT-H INFRARED LAMPS receive FDA 510(k) clearance?

TLC MODELS ULK-H AND ULT-H INFRARED LAMPS received FDA 510(k) clearance on 2003-11-20, under 510(k) number K033035.

Who is the listed applicant for TLC MODELS ULK-H AND ULT-H INFRARED LAMPS?

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

What is the FDA product code for TLC MODELS ULK-H AND ULT-H INFRARED LAMPS?

The FDA product code for TLC MODELS ULK-H AND ULT-H INFRARED LAMPS 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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