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FDA 510(k)

TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE

K-Number: K894084 · 1989-08-17

ApplicantTarget Therapeutics
Decision Date1989-08-17
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1989-08-17 under 510(k) number K894084. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE?

TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE is a medical device that received FDA 510(k) clearance on 1989-08-17. The listed applicant is Target Therapeutics. The 510(k) number is K894084.

When did TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE receive FDA 510(k) clearance?

TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE received FDA 510(k) clearance on 1989-08-17, under 510(k) number K894084.

Who is the listed applicant for TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE?

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 TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE?

The FDA product code for TARGET CATHETERS AND GUIDE WIRES FOR PEDIATRIC USE is DQY.

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Related Devices (Code: DQY)

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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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