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FDA 510(k)

ECHOENCEPHALOGRAPH, DIGITAL, 1000

K-Number: K770575 · 1977-04-26

ApplicantStorz Instrument Co.
Decision Date1977-04-26
Product CodeGXW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ECHOENCEPHALOGRAPH, DIGITAL, 1000 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 1977-04-26 under 510(k) number K770575. The device is classified under product code GXW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHOENCEPHALOGRAPH, DIGITAL, 1000?

ECHOENCEPHALOGRAPH, DIGITAL, 1000 is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Storz Instrument Co.. The 510(k) number is K770575.

When did ECHOENCEPHALOGRAPH, DIGITAL, 1000 receive FDA 510(k) clearance?

ECHOENCEPHALOGRAPH, DIGITAL, 1000 received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770575.

Who is the listed applicant for ECHOENCEPHALOGRAPH, DIGITAL, 1000?

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 ECHOENCEPHALOGRAPH, DIGITAL, 1000?

The FDA product code for ECHOENCEPHALOGRAPH, DIGITAL, 1000 is GXW.

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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: GXW)

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.

K921863SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYSHewlett-Packard Co.K903085SMS-712NAToshiba America Medical Systems, In.CK8534325.0 IOP & 7.5 IOP PROBESDiasonics, Inc.K833522NEURO SECTOR FIXATION DEVICEAdvanced Technology Laboratories, Inc.K821736ECHO-PULSE KM555Rabar, Inc.K770788ECHOENCEPHALOGRAPH, DIGITAL,DIGIECHO2000Storz Instrument Co.

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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