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Vitasystems GmbH

FDA Regulatory Profile

Vitasystems GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 25, 2016.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153477EMMa Electronic Monitoring ManagementMay 25, 2016
K151013Vitaphone Tele ECG Loop RecorderApril 30, 2015
K100383VITAPHONE. MODEL 100 BTApril 20, 2010

FDA data resources