Bard Power-Injectable Implantable Ports (PowerPorts®)
K-Number: K181446 · 2019-07-08
ApplicantC.R. Bard, Inc.
Decision Date2019-07-08
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Bard Power-Injectable Implantable Ports (PowerPorts®) is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2019-07-08 under approval number K181446. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bard Power-Injectable Implantable Ports (PowerPorts®)?
Bard Power-Injectable Implantable Ports (PowerPorts®) is a medical device that received FDA 510(k) clearance on 2019-07-08. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K181446.
When was Bard Power-Injectable Implantable Ports (PowerPorts®) approved by the FDA?
Bard Power-Injectable Implantable Ports (PowerPorts®) received FDA 510(k) clearance on 2019-07-08, under approval number K181446.
What company makes Bard Power-Injectable Implantable Ports (PowerPorts®)?
Bard Power-Injectable Implantable Ports (PowerPorts®) is manufactured by C.R. Bard, Inc..
What is the FDA product code for Bard Power-Injectable Implantable Ports (PowerPorts®)?
The FDA product code for Bard Power-Injectable Implantable Ports (PowerPorts®) is LJT.
Other Devices by C.R. Bard, Inc.
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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.