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FDA 510(k)

SKYTRON EXAM LIGHT

K-Number: K933564 · 1994-02-10

ApplicantSkytron, Div. the Kmw Group, Inc.
Decision Date1994-02-10
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKYTRON EXAM LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Skytron, Div. the Kmw Group, Inc.. It received FDA 510(k) clearance on 1994-02-10 under 510(k) number K933564. 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 SKYTRON EXAM LIGHT?

SKYTRON EXAM LIGHT is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Skytron, Div. the Kmw Group, Inc.. The 510(k) number is K933564.

When did SKYTRON EXAM LIGHT receive FDA 510(k) clearance?

SKYTRON EXAM LIGHT received FDA 510(k) clearance on 1994-02-10, under 510(k) number K933564.

Who is the listed applicant for SKYTRON EXAM LIGHT?

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

What is the FDA product code for SKYTRON EXAM LIGHT?

The FDA product code for SKYTRON EXAM LIGHT is KZF.

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Other records listing Skytron, Div. the Kmw Group, 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.

K071698AURORA LED SERIES SURGICAL LIGHTSK021585STELLAR SERIES SURGICAL LIGHTS WITH HERMESK002463STELLARK992090MILLENNIUM GOLDK950192SKYTRON SKYBOOM SERIESK940616SKYTRON ELITE 3500 TABLE

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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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