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FDA 510(k)

GUIDE WIRE FOR LAPOROSCOPIC USE

K-Number: K926214 · 1993-04-29

ApplicantTerumo Medical Corp.
Decision Date1993-04-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GUIDE WIRE FOR LAPOROSCOPIC USE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1993-04-29 under 510(k) number K926214. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDE WIRE FOR LAPOROSCOPIC USE?

GUIDE WIRE FOR LAPOROSCOPIC USE is a medical device that received FDA 510(k) clearance on 1993-04-29. The listed applicant is Terumo Medical Corp.. The 510(k) number is K926214.

When did GUIDE WIRE FOR LAPOROSCOPIC USE receive FDA 510(k) clearance?

GUIDE WIRE FOR LAPOROSCOPIC USE received FDA 510(k) clearance on 1993-04-29, under 510(k) number K926214.

Who is the listed applicant for GUIDE WIRE FOR LAPOROSCOPIC USE?

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

What is the FDA product code for GUIDE WIRE FOR LAPOROSCOPIC USE?

The FDA product code for GUIDE WIRE FOR LAPOROSCOPIC USE is GCJ.

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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.

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