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FDA 510(k)

INFUSION CATHETER W/SIDE HOLES

K-Number: K854000 · 1985-11-05

ApplicantTarget Therapeutics
Decision Date1985-11-05
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INFUSION CATHETER W/SIDE HOLES is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1985-11-05 under 510(k) number K854000. 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 INFUSION CATHETER W/SIDE HOLES?

INFUSION CATHETER W/SIDE HOLES is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Target Therapeutics. The 510(k) number is K854000.

When did INFUSION CATHETER W/SIDE HOLES receive FDA 510(k) clearance?

INFUSION CATHETER W/SIDE HOLES received FDA 510(k) clearance on 1985-11-05, under 510(k) number K854000.

Who is the listed applicant for INFUSION CATHETER W/SIDE HOLES?

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 INFUSION CATHETER W/SIDE HOLES?

The FDA product code for INFUSION CATHETER W/SIDE HOLES 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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