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Teleemg, LLC USA
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K141524
NEURO-AUDIO
March 12, 2015
K102610
FOCUS EMG DEVICE
March 4, 2011