Alpha Infusion Pump, Model A200, A450

FDA 510(k) K071532 · Advanced Infusion, Inc.

Substantially Equivalent

510(k) numberK071532

Submission

Device name
Alpha Infusion Pump, Model A200, A450
Applicant
Advanced Infusion, Inc.
San Dimas, CA, US
Received
June 5, 2007
Decision date
February 19, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEB – Pump, Infusion, Elastomeric
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

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Questions and answers

When was Alpha Infusion Pump, Model A200, A450 cleared by the FDA?

Alpha Infusion Pump, Model A200, A450 (K071532) received a 510(k) decision of Substantially Equivalent on February 19, 2008, 259 days after the submission was received.

What is the product code of K071532?

The FDA product code is MEB – Pump, Infusion, Elastomeric, a Class II (moderate risk) device regulated under 21 CFR 880.5725.