Cardioquip Modular Cooler-Heater Model MCH-1000

FDA 510(k) K102147 · Cardioquip Llp

Substantially Equivalent

510(k) numberK102147

Submission

Device name
Cardioquip Modular Cooler-Heater Model MCH-1000
Applicant
Cardioquip Llp
Bryan, TX, US
Received
July 30, 2010
Decision date
November 19, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 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).

Other 510(k)s with product code DWC

510(k)DeviceApplicantDecision
K220635Heater-Cooler System 3TDWC · Traditional Livanova Deutschland, GmbH11/16/2022SE
K212657Quantum Heater-CoolerDWC · Traditional Spectrum Medical , Ltd.05/06/2022SE
K191402Heater-Cooler System 3TDWC · Traditional Livanova Deutschland, GmbH02/25/2020SE
K140012Sorin FlexthermDWC · Special Sorin Group Deutschland GmbH01/31/2014SE
K130300Heater-Cooler Unit Hcu 40DWC · Traditional Maquet Cardiopulmonary, AG07/01/2013SE
K122813Hemotherm Model 400CE Cooler/Heater SystemDWC · Traditional Cincinnati Sub-Zero Products, Inc.12/18/2012SE
K071521Terumo HX2 Temperature Management SystemDWC · Traditional Terumo Cardiovascular Systems Corp.11/21/2007SE
K052601Stockert Heater-Cooler System 3TDWC · Traditional Sorin Group Deutschland GmbH06/06/2006SE
K031544Heater Cooler Unit, Model Hcu 30DWC · Traditional Jostra AB08/07/2003SE
K014016Enguard CHC Dual Reservoir Cardioplegia Heater/CoolerDWC · Traditional Minntech Corp.02/01/2002SE

Questions and answers

When was Cardioquip Modular Cooler-Heater Model MCH-1000 cleared by the FDA?

Cardioquip Modular Cooler-Heater Model MCH-1000 (K102147) received a 510(k) decision of Substantially Equivalent on November 19, 2010, 112 days after the submission was received.

What is the product code of K102147?

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