FDA 510(k)

USCI COMMANDER SERIES GUIDE WIRES

K-Number: K961271 · 1996-06-27

Decision Date1996-06-27

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

USCI COMMANDER SERIES GUIDE WIRES 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 1996-06-27 under 510(k) number K961271. 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 COMMANDER SERIES GUIDE WIRES?

USCI COMMANDER SERIES GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1996-06-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K961271.

When did USCI COMMANDER SERIES GUIDE WIRES receive FDA 510(k) clearance?

USCI COMMANDER SERIES GUIDE WIRES received FDA 510(k) clearance on 1996-06-27, under 510(k) number K961271.

Who is the listed applicant for USCI COMMANDER SERIES GUIDE WIRES?

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 COMMANDER SERIES GUIDE WIRES?

The FDA product code for USCI COMMANDER SERIES GUIDE WIRES 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.