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FDA 510(k)

STORZ S6000 LIGHT SOURCE

K-Number: K905376 · 1991-01-23

ApplicantStorz Instrument Co.
Decision Date1991-01-23
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STORZ S6000 LIGHT SOURCE 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 1991-01-23 under 510(k) number K905376. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ S6000 LIGHT SOURCE?

STORZ S6000 LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1991-01-23. The listed applicant is Storz Instrument Co.. The 510(k) number is K905376.

When did STORZ S6000 LIGHT SOURCE receive FDA 510(k) clearance?

STORZ S6000 LIGHT SOURCE received FDA 510(k) clearance on 1991-01-23, under 510(k) number K905376.

Who is the listed applicant for STORZ S6000 LIGHT SOURCE?

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 S6000 LIGHT SOURCE?

The FDA product code for STORZ S6000 LIGHT SOURCE is FCW.

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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: FCW)

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.

K123956POWER LED 175KARL STORZ Endoscopy-America, Inc.K123359OVS1 VIDEO SYSTEMOlive Medical Corp.K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2Richard Wolf Medical Instruments Corp.K093792LED LIGHT SOURCESunoptic Technologies, LLCK091968KARL STORZ LED NOVA 100 COLD LIGHT FOUNTAIN, MODELS 2016020, 20161020CKARL STORZ Endoscopy-America, Inc.K082813STRYKER LED LIGHTSOURCEStryker 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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