Sorin Flextherm

FDA 510(k) K140012 · Sorin Group Deutschland GmbH

Substantially Equivalent

510(k) numberK140012

Submission

Device name
Sorin Flextherm
Applicant
Sorin Group Deutschland GmbH
Arvada, CO, US
Received
January 2, 2014
Decision date
January 31, 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
DWC – Controller, Temperature, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4250
Specialty
Cardiovascular
Life-sustaining
Yes

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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K103168B-CARE5 (B-CARE5 Sensor Module, Venous Sensor, Holder for Measuring Head)DRY · Traditional 01/06/2011SE
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Questions and answers

When was Sorin Flextherm cleared by the FDA?

Sorin Flextherm (K140012) received a 510(k) decision of Substantially Equivalent on January 31, 2014, 29 days after the submission was received.

What is the product code of K140012?

The FDA product code is DWC – Controller, Temperature, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4250.