FDA 510(k)

ECHO-OCULOMETER

K-Number: K771688 · 1977-09-26

Decision Date1977-09-26

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ECHO-OCULOMETER 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 1977-09-26 under 510(k) number K771688. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO-OCULOMETER?

ECHO-OCULOMETER is a medical device that received FDA 510(k) clearance on 1977-09-26. The listed applicant is Storz Instrument Co.. The 510(k) number is K771688.

When did ECHO-OCULOMETER receive FDA 510(k) clearance?

ECHO-OCULOMETER received FDA 510(k) clearance on 1977-09-26, under 510(k) number K771688.

Who is the listed applicant for ECHO-OCULOMETER?

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 ECHO-OCULOMETER?

The FDA product code for ECHO-OCULOMETER is IYO.

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.