K100 Neutral Displacement Needle Free Connector

FDA 510(k) K130023 · Np Medical, Inc.

Substantially Equivalent

510(k) numberK130023

Submission

Device name
K100 Neutral Displacement Needle Free Connector
Applicant
Np Medical, Inc.
South Lyon, MI, US
Received
January 3, 2013
Decision date
April 3, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from B.Braun Medical, Inc.

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Questions and answers

When was K100 Neutral Displacement Needle Free Connector cleared by the FDA?

K100 Neutral Displacement Needle Free Connector (K130023) received a 510(k) decision of Substantially Equivalent on April 3, 2013, 90 days after the submission was received.

What is the product code of K130023?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.