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FDA 510(k)

DOUBLE & SINGLE TANTALUM CLIPS

K-Number: K840207 · 1984-03-29

ApplicantStorz Instrument Co.
Decision Date1984-03-29
Product CodeHQW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DOUBLE & SINGLE TANTALUM CLIPS 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 1984-03-29 under 510(k) number K840207. The device is classified under product code HQW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE & SINGLE TANTALUM CLIPS?

DOUBLE & SINGLE TANTALUM CLIPS is a medical device that received FDA 510(k) clearance on 1984-03-29. The listed applicant is Storz Instrument Co.. The 510(k) number is K840207.

When did DOUBLE & SINGLE TANTALUM CLIPS receive FDA 510(k) clearance?

DOUBLE & SINGLE TANTALUM CLIPS received FDA 510(k) clearance on 1984-03-29, under 510(k) number K840207.

Who is the listed applicant for DOUBLE & SINGLE TANTALUM CLIPS?

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 DOUBLE & SINGLE TANTALUM CLIPS?

The FDA product code for DOUBLE & SINGLE TANTALUM CLIPS is HQW.

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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: HQW)

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.

K897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEPGrieshaber & Co.K901275RETINAL TAAKAlcon Surgical, 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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