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FDA 510(k)

FISHER-PICKERING INTRAOCULAR EYE MAGNET

K-Number: K803194 · 1981-02-04

ApplicantStorz Instrument Co.
Decision Date1981-02-04
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FISHER-PICKERING INTRAOCULAR EYE MAGNET 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 1981-02-04 under 510(k) number K803194. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISHER-PICKERING INTRAOCULAR EYE MAGNET?

FISHER-PICKERING INTRAOCULAR EYE MAGNET is a medical device that received FDA 510(k) clearance on 1981-02-04. The listed applicant is Storz Instrument Co.. The 510(k) number is K803194.

When did FISHER-PICKERING INTRAOCULAR EYE MAGNET receive FDA 510(k) clearance?

FISHER-PICKERING INTRAOCULAR EYE MAGNET received FDA 510(k) clearance on 1981-02-04, under 510(k) number K803194.

Who is the listed applicant for FISHER-PICKERING INTRAOCULAR EYE MAGNET?

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 FISHER-PICKERING INTRAOCULAR EYE MAGNET?

The FDA product code for FISHER-PICKERING INTRAOCULAR EYE MAGNET is HNR.

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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: HNR)

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.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, 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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