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FDA 510(k)

STORZ FIBEROPTIC ENDO-ILLUMINATORS

K-Number: K896549 · 1990-02-15

ApplicantStorz Instrument Co.
Decision Date1990-02-15
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STORZ FIBEROPTIC ENDO-ILLUMINATORS 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 1990-02-15 under 510(k) number K896549. The device is classified under product code HBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ FIBEROPTIC ENDO-ILLUMINATORS?

STORZ FIBEROPTIC ENDO-ILLUMINATORS is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Storz Instrument Co.. The 510(k) number is K896549.

When did STORZ FIBEROPTIC ENDO-ILLUMINATORS receive FDA 510(k) clearance?

STORZ FIBEROPTIC ENDO-ILLUMINATORS received FDA 510(k) clearance on 1990-02-15, under 510(k) number K896549.

Who is the listed applicant for STORZ FIBEROPTIC ENDO-ILLUMINATORS?

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 FIBEROPTIC ENDO-ILLUMINATORS?

The FDA product code for STORZ FIBEROPTIC ENDO-ILLUMINATORS is HBI.

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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: HBI)

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.

K223183Light-Guide CablesOlympus Winter & Ibe GmbHK163185OptiLux LED IlluminatorIsolux, LLCK111342LIGHT GUIDE CABLESchott North AmericaK0529791125 XSB XENON FIBER-OPTIC LIGHT SOURCEIsolux, LLCK021931ENDOSCOPIC FIBEROPTIC CABLEGulf Medical FiberopticsK991208ENDOSCOPIC FIBEROPTIC CABLEIsolux America

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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