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FDA 510(k)

TRACKER-25 INFUSION CATHETER

K-Number: K874751 · 1988-02-12

ApplicantTarget Therapeutics
Decision Date1988-02-12
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRACKER-25 INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K874751. 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 TRACKER-25 INFUSION CATHETER?

TRACKER-25 INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Target Therapeutics. The 510(k) number is K874751.

When did TRACKER-25 INFUSION CATHETER receive FDA 510(k) clearance?

TRACKER-25 INFUSION CATHETER received FDA 510(k) clearance on 1988-02-12, under 510(k) number K874751.

Who is the listed applicant for TRACKER-25 INFUSION CATHETER?

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 TRACKER-25 INFUSION CATHETER?

The FDA product code for TRACKER-25 INFUSION CATHETER is 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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