FDA 510(k)

OLYMPUS GUIDE WIRE

K-Number: K933110 · 1993-11-04

Decision Date1993-11-04

Product CodeOCY

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

OLYMPUS GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1993-11-04 under 510(k) number K933110. The device is classified under product code OCY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS GUIDE WIRE?

OLYMPUS GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1993-11-04. The listed applicant is Olympus Corp.. The 510(k) number is K933110.

When did OLYMPUS GUIDE WIRE receive FDA 510(k) clearance?

OLYMPUS GUIDE WIRE received FDA 510(k) clearance on 1993-11-04, under 510(k) number K933110.

Who is the listed applicant for OLYMPUS GUIDE WIRE?

The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS GUIDE WIRE?

The FDA product code for OLYMPUS GUIDE WIRE is OCY.

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Other records listing Olympus Corp. as applicant

K915402EW-10 AND EW-20 K933200OLYMPUS PBD STENTS K942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES K931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS K934835FLOVAL K931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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Related Devices (Code: OCY)

K153264EasyPass GuidewireMedi-Globe Corporation K131072ORCHESTRA HYDROPHILIC GUIDEWIRE STANDARD ANGLED, ORCHESTRA HYDROPHILIC GUIDEWIRE STRAIGHT STIFF, ORCHESTRA HYDROPHILICColoplast A/S K124052OSTAVI HYDROPHILIC GUIDEWIRELake Region Medical K123438XENX STONE MANAGEMENT DEVICEXenolith Medical K123439NEO ERCP GUIDEWIRENeometrics, Inc.K122816AXCESS SOFT TIP WIRE GUIDEWilson-Cook Medical, Inc.

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.