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FDA 510(k)

STORZ CORNEO-SCAN II CS2000

K-Number: K844477 · 1985-01-23

ApplicantStorz Instrument Co.
Decision Date1985-01-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STORZ CORNEO-SCAN II CS2000 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 1985-01-23 under 510(k) number K844477. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ CORNEO-SCAN II CS2000?

STORZ CORNEO-SCAN II CS2000 is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is Storz Instrument Co.. The 510(k) number is K844477.

When did STORZ CORNEO-SCAN II CS2000 receive FDA 510(k) clearance?

STORZ CORNEO-SCAN II CS2000 received FDA 510(k) clearance on 1985-01-23, under 510(k) number K844477.

Who is the listed applicant for STORZ CORNEO-SCAN II CS2000?

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 CORNEO-SCAN II CS2000?

The FDA product code for STORZ CORNEO-SCAN II CS2000 is IYO.

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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: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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