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Pmt Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
5
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K202542Allura Vaginal StentSeptember 30, 2020
K151790PMT Platinum Depthalon Depth ElectrodeJuly 14, 2016