Devices

Revision K Actuator Test Boards

Model / Serial
Revision K Actuator Test Boards
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
USA (nationwide) and the country of Canada.*
Product Description
Revision K Actuator Test Boards sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T). || Part Number: 190713 Revision K
Manufacturer
Fresenius Medical Care Holdings, Inc.
1 Event
- Recall of Revision K Actuator Test Boards

Manufacturer

Fresenius Medical Care Holdings, Inc.

Manufacturer Address
Fresenius Medical Care Holdings, Inc., 920 Winter St, Waltham MA 02451-1521
Manufacturer Parent Company (2017)
Fresenius SE & Co KGaA
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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