Hickman TriFusion Catheter
K-Number: K172511 · 2018-04-20
ApplicantC.R. Bard, Inc.
Decision Date2018-04-20
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Hickman TriFusion Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2018-04-20 under approval number K172511. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Hickman TriFusion Catheter?
Hickman TriFusion Catheter is a medical device that received FDA 510(k) clearance on 2018-04-20. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K172511.
When was Hickman TriFusion Catheter approved by the FDA?
Hickman TriFusion Catheter received FDA 510(k) clearance on 2018-04-20, under approval number K172511.
What company makes Hickman TriFusion Catheter?
Hickman TriFusion Catheter is manufactured by C.R. Bard, Inc..
What is the FDA product code for Hickman TriFusion Catheter?
The FDA product code for Hickman TriFusion Catheter is LJS.
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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.