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FDA 510(k)

NITINOL SEEKER(R) GUIDE WIRES

K-Number: K914032 · 1992-02-11

ApplicantTarget Therapeutics
Decision Date1992-02-11
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NITINOL SEEKER(R) 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 1992-02-11 under 510(k) number K914032. 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 NITINOL SEEKER(R) GUIDE WIRES?

NITINOL SEEKER(R) GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Target Therapeutics. The 510(k) number is K914032.

When did NITINOL SEEKER(R) GUIDE WIRES receive FDA 510(k) clearance?

NITINOL SEEKER(R) GUIDE WIRES received FDA 510(k) clearance on 1992-02-11, under 510(k) number K914032.

Who is the listed applicant for NITINOL SEEKER(R) 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 NITINOL SEEKER(R) GUIDE WIRES?

The FDA product code for NITINOL SEEKER(R) 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.

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