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Hocoma AG

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Ko recall (Z-2418-2020)Hocoma AG2020-06-23
Hocoma Lokomat-System with Pediatric Module Software Versions: V4.30, V4.31, V4.31a, V4.31 recall (Z-0590-2010)Hocoma AG2010-01-07

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