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Promedtek, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162240ProMedTek Model C1400 Shortwave Diathermy DeviceNovember 17, 2016
K070931MODEL PMT850May 24, 2007