FDA 510(k)

STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK

K-Number: K961874 · 1996-08-06

Decision Date1996-08-06

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK 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 1996-08-06 under 510(k) number K961874. 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 DP5100 ANTERIOR COLLECTION CASSETTE PACK?

STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK is a medical device that received FDA 510(k) clearance on 1996-08-06. The listed applicant is Storz Instrument Co.. The 510(k) number is K961874.

When did STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK receive FDA 510(k) clearance?

STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK received FDA 510(k) clearance on 1996-08-06, under 510(k) number K961874.

Who is the listed applicant for STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK?

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 DP5100 ANTERIOR COLLECTION CASSETTE PACK?

The FDA product code for STORZ DP5100 ANTERIOR COLLECTION CASSETTE PACK 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.