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Obmedical Company
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K190798
LaborView LV1000 Wireless Electrode System
September 18, 2020
K142583
LaborView LV1000
January 16, 2015