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Rz Medizintechnik GmbH

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K243382RZ Resectoscope SystemJune 3, 2025
K130778DISCOSCOPES, CERVICAL ENDOSCOPESApril 14, 2014
K082902RZ ENDOSCOPIC (MINIMALLY INVASIVE) INSTRUMENTS AND ACCESSORIESDecember 10, 2008