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FDA 510(k)

MASTERPIECES(TM)/MICRO/MINI SYSTEMS

K-Number: K913289 · 1991-09-05

ApplicantStorz Instrument Co.
Decision Date1991-09-05
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MASTERPIECES(TM)/MICRO/MINI SYSTEMS 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 1991-09-05 under 510(k) number K913289. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERPIECES(TM)/MICRO/MINI SYSTEMS?

MASTERPIECES(TM)/MICRO/MINI SYSTEMS is a medical device that received FDA 510(k) clearance on 1991-09-05. The listed applicant is Storz Instrument Co.. The 510(k) number is K913289.

When did MASTERPIECES(TM)/MICRO/MINI SYSTEMS receive FDA 510(k) clearance?

MASTERPIECES(TM)/MICRO/MINI SYSTEMS received FDA 510(k) clearance on 1991-09-05, under 510(k) number K913289.

Who is the listed applicant for MASTERPIECES(TM)/MICRO/MINI SYSTEMS?

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 MASTERPIECES(TM)/MICRO/MINI SYSTEMS?

The FDA product code for MASTERPIECES(TM)/MICRO/MINI SYSTEMS is HRS.

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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: HRS)

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.

K261892ProRib Fixation SystemCosta Surgical, Inc.K262098EnHAnce PEEK Bunion SystemNvision Biomedical TechnologiesK262963TMC Implant Fixation SystemTreace Medical Concepts, Inc.K261647Tempo Plating System; Ultra Compression Screw SystemPace SurgicalK261830FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See Catalog);FRAXION Mini Plate System (Various - See Catalog);FRAXION Bone Screw System (Various - See Catalog)Ortler Global Tibbi Gerecler Anonim SirketiK262537Versalock Sterile Plating SystemGM Dos Reis Industria e Comercio Ltda.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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