Dannoritzer Medizintechnik GmbH & Co. KG

FDA Regulatory Profile

Summary

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

Recent Recalls

NumberClassProductDate
Z-0062-2019Class IIILaparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) InseAugust 6, 2018

Recent 510(k) Clearances

K-NumberDeviceDate
K052759DAN MONOPOLAR LAP ACCESSORIESJune 14, 2006