Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector

FDA 510(k) K213089 · Ivenix, Inc.

Substantially Equivalent

510(k) numberK213089

Submission

Device name
Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector
Applicant
Ivenix, Inc.
North Andover, MA, US
Received
September 24, 2021
Decision date
November 10, 2021
Decision
Substantially Equivalent (SESE)
Type
Special 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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Questions and answers

When was Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector cleared by the FDA?

Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector (K213089) received a 510(k) decision of Substantially Equivalent on November 10, 2021, 47 days after the submission was received.

What is the product code of K213089?

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