Decision Date1981-03-05
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
USCI CARDIOVASCULAR 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 1981-03-05 under 510(k) number K810412. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the USCI CARDIOVASCULAR CATHETER?
USCI CARDIOVASCULAR CATHETER is a medical device that received FDA 510(k) clearance on 1981-03-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K810412.
When did USCI CARDIOVASCULAR CATHETER receive FDA 510(k) clearance?
USCI CARDIOVASCULAR CATHETER received FDA 510(k) clearance on 1981-03-05, under 510(k) number K810412.
Who is the listed applicant for USCI CARDIOVASCULAR 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 CARDIOVASCULAR CATHETER?
The FDA product code for USCI CARDIOVASCULAR CATHETER is DQO.
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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.