FDA 510(k)

REMOVE LABELING RESTRICT FROM GUIDE WIRES

K-Number: K912293 · 1991-12-05

Decision Date1991-12-05

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

REMOVE LABELING RESTRICT FROM GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1991-12-05 under 510(k) number K912293. 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 REMOVE LABELING RESTRICT FROM GUIDE WIRES?

REMOVE LABELING RESTRICT FROM GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1991-12-05. The listed applicant is Target Therapeutics. The 510(k) number is K912293.

When did REMOVE LABELING RESTRICT FROM GUIDE WIRES receive FDA 510(k) clearance?

REMOVE LABELING RESTRICT FROM GUIDE WIRES received FDA 510(k) clearance on 1991-12-05, under 510(k) number K912293.

Who is the listed applicant for REMOVE LABELING RESTRICT FROM GUIDE WIRES?

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

What is the FDA product code for REMOVE LABELING RESTRICT FROM GUIDE WIRES?

The FDA product code for REMOVE LABELING RESTRICT FROM 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.