FDA 510(k)

PowerMidline Catheter

K-Number: K162900 · 2016-12-14

Decision Date2016-12-14

Product CodePND

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PowerMidline 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 2016-12-14 under 510(k) number K162900. 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 2016-12-14. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162900.

When did PowerMidline Catheter receive FDA 510(k) clearance?

PowerMidline Catheter received FDA 510(k) clearance on 2016-12-14, under 510(k) number K162900.

Who is the listed applicant for PowerMidline 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 PowerMidline Catheter?

The FDA product code for PowerMidline Catheter is PND.

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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.