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FDA 510(k)

INFRARED LAMP

K-Number: K925054 · 1993-06-29

ApplicantLumiscope Co., Inc.
Decision Date1993-06-29
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 Lumiscope Co., Inc.. It received FDA 510(k) clearance on 1993-06-29 under 510(k) number K925054. 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 1993-06-29. The listed applicant is Lumiscope Co., Inc.. The 510(k) number is K925054.

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

INFRARED LAMP received FDA 510(k) clearance on 1993-06-29, under 510(k) number K925054.

Who is the listed applicant for INFRARED LAMP?

The FDA 510(k) record lists Lumiscope Co., 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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Other records listing Lumiscope Co., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K032714CARDICARE MODEL MT-301F & MT-301CK954792LUMISCOPE MODEL 2018 THERMOMETERK931768INTERFERENTIAL CURRENT THERAPY UNITK924081LUMISONICK920099GYMMANK901849LUMISCOPE EMS 8000

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Related Devices (Code: ILY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253965CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)Wuhan PHOMED Technology Company , Ltd.K242755Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B)Gigaalaser Company , Ltd.K231997SIRONA 100 Therapy Laser System (OEM's Model EVANLAS)Cure Point Therapeutics, Inc.K223642LED Lip Perfector, model: ZC-05Light Tree Ventures Europe B.V.K221189OLIZ LTB-1000ALtbio Co., Ltd.K213524CytonPro-5000Cytonsys, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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