FDA 510(k)

USCI ADJUSTABLE TIP GUIDE WIRE

K-Number: K884647 · 1989-01-12

Decision Date1989-01-12

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

USCI ADJUSTABLE TIP 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 1989-01-12 under 510(k) number K884647. 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 ADJUSTABLE TIP GUIDE WIRE?

USCI ADJUSTABLE TIP GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1989-01-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K884647.

When did USCI ADJUSTABLE TIP GUIDE WIRE receive FDA 510(k) clearance?

USCI ADJUSTABLE TIP GUIDE WIRE received FDA 510(k) clearance on 1989-01-12, under 510(k) number K884647.

Who is the listed applicant for USCI ADJUSTABLE TIP 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 ADJUSTABLE TIP GUIDE WIRE?

The FDA product code for USCI ADJUSTABLE TIP GUIDE WIRE is DQX.

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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.