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Pausch Medical GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221949Ortho Device, ADAPTIX 3D Orthopedic Imaging SystemJanuary 26, 2023
K180651Uroview FD IIApril 12, 2018
K161019Uroview FDAugust 17, 2016