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Vitasystems GmbH
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K153477
EMMa Electronic Monitoring Management
May 25, 2016
K151013
Vitaphone Tele ECG Loop Recorder
April 30, 2015
K100383
VITAPHONE. MODEL 100 BT
April 20, 2010