Affinity Pixie Oxygenation System with; Carmeda Bioactive Surface, Balance Biosuface

FDA 510(k) K141233 · Medtronic, Inc.

Substantially Equivalent

510(k) numberK141233

Submission

Device name
Affinity Pixie Oxygenation System with; Carmeda Bioactive Surface, Balance Biosuface
Applicant
Medtronic, Inc.
Minneapolis, MN, US
Received
May 13, 2014
Decision date
June 12, 2014
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTN – Reservoir, Blood, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4400
Specialty
Cardiovascular

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Questions and answers

When was Affinity Pixie Oxygenation System with; Carmeda Bioactive Surface, Balance Biosuface cleared by the FDA?

Affinity Pixie Oxygenation System with; Carmeda Bioactive Surface, Balance Biosuface (K141233) received a 510(k) decision of Substantially Equivalent on June 12, 2014, 30 days after the submission was received.

What is the product code of K141233?

The FDA product code is DTN – Reservoir, Blood, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4400.