Decision Date1990-04-23
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
USCI 7F LARGE LUMEN GUIDING 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 1990-04-23 under 510(k) number K895180. 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 7F LARGE LUMEN GUIDING CATHETER?
USCI 7F LARGE LUMEN GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K895180.
When did USCI 7F LARGE LUMEN GUIDING CATHETER receive FDA 510(k) clearance?
USCI 7F LARGE LUMEN GUIDING CATHETER received FDA 510(k) clearance on 1990-04-23, under 510(k) number K895180.
Who is the listed applicant for USCI 7F LARGE LUMEN GUIDING 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 7F LARGE LUMEN GUIDING CATHETER?
The FDA product code for USCI 7F LARGE LUMEN GUIDING 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.