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FDA 510(k)

MI-5 DIAGNOSTIC LIGHT

K-Number: K931026 · 1993-08-19

ApplicantMedical Illumination, Inc.
Decision Date1993-08-19
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MI-5 DIAGNOSTIC LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Illumination, Inc.. It received FDA 510(k) clearance on 1993-08-19 under 510(k) number K931026. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MI-5 DIAGNOSTIC LIGHT?

MI-5 DIAGNOSTIC LIGHT is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is Medical Illumination, Inc.. The 510(k) number is K931026.

When did MI-5 DIAGNOSTIC LIGHT receive FDA 510(k) clearance?

MI-5 DIAGNOSTIC LIGHT received FDA 510(k) clearance on 1993-08-19, under 510(k) number K931026.

Who is the listed applicant for MI-5 DIAGNOSTIC LIGHT?

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

What is the FDA product code for MI-5 DIAGNOSTIC LIGHT?

The FDA product code for MI-5 DIAGNOSTIC LIGHT is KZF.

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Other records listing Medical Illumination, 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.

K931646MI-4 VARIABLE SPOT LIGHTK930897MI-15 EXAM SURGICAL LIGHTK925710M.E.D. LIGHTK922278ILLUMINATOR IIIK922282ILLUMINATOR VIII ULTRA/SPOTK922277ILLUMINATOR II

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Related Devices (Code: KZF)

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.

K954943NEVOSCOPENizar A. MullaniK952835WELCH ALLYN VIDEO EPISCOPEWelch Allyn, Inc.K945507H 5100, H 5200, H 5300Rudolf Riester GmbH & Co. KGK941869SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEGThe Lighthouse For the Blind, Inc.K936088WAVE FLUORESCENT MAGNIFIERBurton Medical Products Corp.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.

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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