PowerMidline Catheter
K-Number: K153393 · 2016-06-28
ApplicantC.R. Bard, Inc.
Decision Date2016-06-28
Product CodePND
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
PowerMidline Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-06-28 under approval number K153393. The device is classified under product code PND. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PowerMidline Catheter?
PowerMidline Catheter is a medical device that received FDA 510(k) clearance on 2016-06-28. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K153393.
When was PowerMidline Catheter approved by the FDA?
PowerMidline Catheter received FDA 510(k) clearance on 2016-06-28, under approval number K153393.
What company makes PowerMidline Catheter?
PowerMidline Catheter is manufactured by C.R. Bard, Inc..
What is the FDA product code for PowerMidline Catheter?
The FDA product code for PowerMidline Catheter is PND.
Other Devices by C.R. Bard, Inc.
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K170158PowerGlide ST Midline CatheterC.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.