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FDA 510(k)

USCI CORONARY INFUSION CATHETER

K-Number: K891069 · 1989-08-09

ApplicantC.R. Bard, Inc.
Decision Date1989-08-09
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI CORONARY INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1989-08-09 under 510(k) number K891069. 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 USCI CORONARY INFUSION CATHETER?

USCI CORONARY INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1989-08-09. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K891069.

When did USCI CORONARY INFUSION CATHETER receive FDA 510(k) clearance?

USCI CORONARY INFUSION CATHETER received FDA 510(k) clearance on 1989-08-09, under 510(k) number K891069.

Who is the listed applicant for USCI CORONARY INFUSION CATHETER?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for USCI CORONARY INFUSION CATHETER?

The FDA product code for USCI CORONARY 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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