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FDA 510(k)

RITTER MODEL 158 AND 159 EXAM LIGHTS

K-Number: K932719 · 1993-12-02

ApplicantMidmark Corp.
Decision Date1993-12-02
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RITTER MODEL 158 AND 159 EXAM LIGHTS is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1993-12-02 under 510(k) number K932719. 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 RITTER MODEL 158 AND 159 EXAM LIGHTS?

RITTER MODEL 158 AND 159 EXAM LIGHTS is a medical device that received FDA 510(k) clearance on 1993-12-02. The listed applicant is Midmark Corp.. The 510(k) number is K932719.

When did RITTER MODEL 158 AND 159 EXAM LIGHTS receive FDA 510(k) clearance?

RITTER MODEL 158 AND 159 EXAM LIGHTS received FDA 510(k) clearance on 1993-12-02, under 510(k) number K932719.

Who is the listed applicant for RITTER MODEL 158 AND 159 EXAM LIGHTS?

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

What is the FDA product code for RITTER MODEL 158 AND 159 EXAM LIGHTS?

The FDA product code for RITTER MODEL 158 AND 159 EXAM LIGHTS is KZF.

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Other records listing Midmark 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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

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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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