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FDA 510(k)

STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE

K-Number: K854587 · 1986-02-04

ApplicantStorz Instrument Co.
Decision Date1986-02-04
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE 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 1986-02-04 under 510(k) number K854587. 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 MVS DISPOSABLE FIBEROPTIC LIGHTPIPE?

STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Storz Instrument Co.. The 510(k) number is K854587.

When did STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE receive FDA 510(k) clearance?

STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854587.

Who is the listed applicant for STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE?

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 MVS DISPOSABLE FIBEROPTIC LIGHTPIPE?

The FDA product code for STORZ MVS DISPOSABLE FIBEROPTIC LIGHTPIPE 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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