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FDA 510(k)

STORZ MILLENNIUM VISCOUS FLUID SYSTEM

K-Number: K972664 · 1997-10-10

ApplicantStorz Instrument Co.
Decision Date1997-10-10
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STORZ MILLENNIUM VISCOUS FLUID SYSTEM 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 1997-10-10 under 510(k) number K972664. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ MILLENNIUM VISCOUS FLUID SYSTEM?

STORZ MILLENNIUM VISCOUS FLUID SYSTEM is a medical device that received FDA 510(k) clearance on 1997-10-10. The listed applicant is Storz Instrument Co.. The 510(k) number is K972664.

When did STORZ MILLENNIUM VISCOUS FLUID SYSTEM receive FDA 510(k) clearance?

STORZ MILLENNIUM VISCOUS FLUID SYSTEM received FDA 510(k) clearance on 1997-10-10, under 510(k) number K972664.

Who is the listed applicant for STORZ MILLENNIUM VISCOUS FLUID SYSTEM?

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 MILLENNIUM VISCOUS FLUID SYSTEM?

The FDA product code for STORZ MILLENNIUM VISCOUS FLUID SYSTEM is MRH.

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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 SYSTEMK971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLESK964743STORZ E8010 ERGOTEC/PREMIERE ADAPTORK960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCHK960061STORZ D7108 MICROSCISSORS HANDPIECE/STORZ D7106 MICROSCISSORS DRIVE TUBE

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Related Devices (Code: MRH)

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.

K253760OMNI Ultra Surgical System (1-110)Sight Sciences, Inc.K243503VIA360™ Surgical SystemNew World Medical, Inc.K232214OMNI Surgical SystemSight Sciences, Inc.K213173TrabEx ProMicrosurgical Technologies, Inc.K212797iPrime Viscodelivery SystemGlaukosK211680Streamline Surgical SystemNew World Medical, 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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