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FDA 510(k)

WAVE FLUORESCENT MAGNIFIER

K-Number: K936088 · 1994-04-26

ApplicantBurton Medical Products Corp.
Decision Date1994-04-26
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WAVE FLUORESCENT MAGNIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Burton Medical Products Corp.. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K936088. 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 WAVE FLUORESCENT MAGNIFIER?

WAVE FLUORESCENT MAGNIFIER is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Burton Medical Products Corp.. The 510(k) number is K936088.

When did WAVE FLUORESCENT MAGNIFIER receive FDA 510(k) clearance?

WAVE FLUORESCENT MAGNIFIER received FDA 510(k) clearance on 1994-04-26, under 510(k) number K936088.

Who is the listed applicant for WAVE FLUORESCENT MAGNIFIER?

The FDA 510(k) record lists Burton Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WAVE FLUORESCENT MAGNIFIER?

The FDA product code for WAVE FLUORESCENT MAGNIFIER is KZF.

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Other records listing Burton Medical Products Corp. 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.

K101537AIM 200, MAJOR SURGICAL LIGHTK042395OUTPATIENT III MINOR SURGERY LIGHTK000639VISIONARY 2000K963682GENIE' SINGLE CEILING AND DOUBLE CEILINGK961843GENIEK935102SATURN LIGHT

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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.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.K933564SKYTRON EXAM LIGHTSkytron, Div. the Kmw Group, 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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