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FDA 510(k)

STORZ #6500 POWER EXAMINATION CHAIR

K-Number: K820636 · 1982-03-26

ApplicantStorz Instrument Co.
Decision Date1982-03-26
Product CodeGBB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STORZ #6500 POWER EXAMINATION CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1982-03-26 under 510(k) number K820636. The device is classified under product code GBB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ #6500 POWER EXAMINATION CHAIR?

STORZ #6500 POWER EXAMINATION CHAIR is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Storz Instrument Co.. The 510(k) number is K820636.

When did STORZ #6500 POWER EXAMINATION CHAIR receive FDA 510(k) clearance?

STORZ #6500 POWER EXAMINATION CHAIR received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820636.

Who is the listed applicant for STORZ #6500 POWER EXAMINATION CHAIR?

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

What is the FDA product code for STORZ #6500 POWER EXAMINATION CHAIR?

The FDA product code for STORZ #6500 POWER EXAMINATION CHAIR is GBB.

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Other records listing Storz 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.

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKK980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEMK972664STORZ MILLENNIUM VISCOUS FLUID SYSTEMK971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLESK964743STORZ E8010 ERGOTEC/PREMIERE ADAPTORK960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

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Related Devices (Code: GBB)

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.

K964102TENET TIBIAL FRACTURE SUPPORTTenet Medical EngineeringK893598HYDRAULIC FOOT OPERATED STOOLArthro-Medic, Inc.K831385LITHOTOMY CHAIR #415Midmark Corp.K831325NUTROMATMedlog GmbH Marketing ServicesK822264NAGASHIMA SN OPERATOR'S CHAIRKelleher Corp.K822251EXAMINATION & TREATMENT CHAIRSKelleher 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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