VBM Medizintechnik GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K200190ScalpelCricOctober 30, 2020
K112783MANUJET IIIDecember 22, 2011
K955461TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).March 19, 1997