FDA 510(k)

STORZ MICROSURGICAL BIPOLAR COAGULATOR

K-Number: K883060 · 1988-08-03

Decision Date1988-08-03

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STORZ MICROSURGICAL BIPOLAR COAGULATOR 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 1988-08-03 under 510(k) number K883060. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ MICROSURGICAL BIPOLAR COAGULATOR?

STORZ MICROSURGICAL BIPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is Storz Instrument Co.. The 510(k) number is K883060.

When did STORZ MICROSURGICAL BIPOLAR COAGULATOR receive FDA 510(k) clearance?

STORZ MICROSURGICAL BIPOLAR COAGULATOR received FDA 510(k) clearance on 1988-08-03, under 510(k) number K883060.

Who is the listed applicant for STORZ MICROSURGICAL BIPOLAR COAGULATOR?

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 MICROSURGICAL BIPOLAR COAGULATOR?

The FDA product code for STORZ MICROSURGICAL BIPOLAR COAGULATOR is GEI.

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Other records listing Storz Instrument Co. as applicant

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACK K980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM K972664STORZ MILLENNIUM VISCOUS FLUID SYSTEM K971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLES K964743STORZ E8010 ERGOTEC/PREMIERE ADAPTOR K960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

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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.