Intravascular Administration Sets

FDA 510(k) K203609 · Baxter Healthcare Corporation

Substantially Equivalent

510(k) numberK203609

Submission

Device name
Intravascular Administration Sets
Applicant
Baxter Healthcare Corporation
Round Lake, IL, US
Received
December 10, 2020
Decision date
September 30, 2021
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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Questions and answers

When was Intravascular Administration Sets cleared by the FDA?

Intravascular Administration Sets (K203609) received a 510(k) decision of Substantially Equivalent on September 30, 2021, 294 days after the submission was received.

What is the product code of K203609?

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