Gebauer Medizintechnik GmbH

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K072102EPIVISION SL SYSTEMJanuary 16, 2009
K041206EPITOME SYSTEMSeptember 15, 2004