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FDA 510(k)

DEPUY (NITINO) GUIDE WIRE

K-Number: K914693 · 1991-12-09

ApplicantDepuy, Inc.
Decision Date1991-12-09
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY (NITINO) GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1991-12-09 under 510(k) number K914693. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY (NITINO) GUIDE WIRE?

DEPUY (NITINO) GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Depuy, Inc.. The 510(k) number is K914693.

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

DEPUY (NITINO) GUIDE WIRE received FDA 510(k) clearance on 1991-12-09, under 510(k) number K914693.

Who is the listed applicant for DEPUY (NITINO) GUIDE WIRE?

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

What is the FDA product code for DEPUY (NITINO) GUIDE WIRE?

The FDA product code for DEPUY (NITINO) GUIDE WIRE is JDQ.

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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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