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FDA 510(k)

TINY HALOGEN EXAM LIGHT

K-Number: K896962 · 1989-12-29

ApplicantJedmed Instrument Co.
Decision Date1989-12-29
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TINY HALOGEN EXAM LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1989-12-29 under 510(k) number K896962. 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 TINY HALOGEN EXAM LIGHT?

TINY HALOGEN EXAM LIGHT is a medical device that received FDA 510(k) clearance on 1989-12-29. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K896962.

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

TINY HALOGEN EXAM LIGHT received FDA 510(k) clearance on 1989-12-29, under 510(k) number K896962.

Who is the listed applicant for TINY HALOGEN EXAM LIGHT?

The FDA 510(k) record lists Jedmed Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TINY HALOGEN EXAM LIGHT?

The FDA product code for TINY HALOGEN EXAM LIGHT is KZF.

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Other records listing Jedmed Instrument Co. 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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K953457JEDMED SPECTRUM ENT CABINETK950925JEDMED LARYNGEAL SCOPEK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

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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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