FDA 510(k)

USCI(R) SILK (TM) GUIDE WIRE

K-Number: K903923 · 1990-11-21

Decision Date1990-11-21

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

USCI(R) SILK (TM) GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1990-11-21 under 510(k) number K903923. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI(R) SILK (TM) GUIDE WIRE?

USCI(R) SILK (TM) GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1990-11-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K903923.

When did USCI(R) SILK (TM) GUIDE WIRE receive FDA 510(k) clearance?

USCI(R) SILK (TM) GUIDE WIRE received FDA 510(k) clearance on 1990-11-21, under 510(k) number K903923.

Who is the listed applicant for USCI(R) SILK (TM) GUIDE WIRE?

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

What is the FDA product code for USCI(R) SILK (TM) GUIDE WIRE?

The FDA product code for USCI(R) SILK (TM) GUIDE WIRE is DQX.

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Official Source

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