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FDA 510(k)

STORZ E9050 & E9055 DIAMOND KNIVES

K-Number: K861732 · 1986-05-28

ApplicantStorz Instrument Co.
Decision Date1986-05-28
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STORZ E9050 & E9055 DIAMOND KNIVES 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 1986-05-28 under 510(k) number K861732. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ E9050 & E9055 DIAMOND KNIVES?

STORZ E9050 & E9055 DIAMOND KNIVES is a medical device that received FDA 510(k) clearance on 1986-05-28. The listed applicant is Storz Instrument Co.. The 510(k) number is K861732.

When did STORZ E9050 & E9055 DIAMOND KNIVES receive FDA 510(k) clearance?

STORZ E9050 & E9055 DIAMOND KNIVES received FDA 510(k) clearance on 1986-05-28, under 510(k) number K861732.

Who is the listed applicant for STORZ E9050 & E9055 DIAMOND KNIVES?

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 E9050 & E9055 DIAMOND KNIVES?

The FDA product code for STORZ E9050 & E9055 DIAMOND KNIVES is HNN.

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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: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, 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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