FDA 510(k)

STORZ I/A HANDPIECES

K-Number: K951463 · 1995-10-27

Decision Date1995-10-27

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

STORZ I/A HANDPIECES 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 1995-10-27 under 510(k) number K951463. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ I/A HANDPIECES?

STORZ I/A HANDPIECES is a medical device that received FDA 510(k) clearance on 1995-10-27. The listed applicant is Storz Instrument Co.. The 510(k) number is K951463.

When did STORZ I/A HANDPIECES receive FDA 510(k) clearance?

STORZ I/A HANDPIECES received FDA 510(k) clearance on 1995-10-27, under 510(k) number K951463.

Who is the listed applicant for STORZ I/A HANDPIECES?

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 I/A HANDPIECES?

The FDA product code for STORZ I/A HANDPIECES is HQC.

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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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Related Devices (Code: HQC)

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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.