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Stockert GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K070336STOCKERT NEURO N50, MODEL12267June 14, 2007
K070134MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098March 22, 2007
K061983STIMUPLEX PENNovember 21, 2006
K052313STIMUPLEX HNS-12, MODEL 4892098November 17, 2005
K003983STIMUPLEX HNS-11June 6, 2001