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FDA 510(k)

INFRARED LAMP

K-Number: K922900 · 1992-11-24

ApplicantHarrier, Inc.
Decision Date1992-11-24
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INFRARED LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Harrier, Inc.. It received FDA 510(k) clearance on 1992-11-24 under 510(k) number K922900. 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 INFRARED LAMP?

INFRARED LAMP is a medical device that received FDA 510(k) clearance on 1992-11-24. The listed applicant is Harrier, Inc.. The 510(k) number is K922900.

When did INFRARED LAMP receive FDA 510(k) clearance?

INFRARED LAMP received FDA 510(k) clearance on 1992-11-24, under 510(k) number K922900.

Who is the listed applicant for INFRARED LAMP?

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

What is the FDA product code for INFRARED LAMP?

The FDA product code for INFRARED LAMP 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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