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FDA 510(k) Applications Submitted by DOMINIKA SCHULER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070134
01/16/2007
MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098
STOCKERT GMBH
K070336
02/05/2007
STOCKERT NEURO N50, MODEL12267
STOCKERT GMBH
K061983
07/13/2006
STIMUPLEX PEN
STOCKERT GMBH
K052313
08/25/2005
STIMUPLEX HNS-12, MODEL 4892098
STOCKERT GMBH
K003983
12/26/2000
STIMUPLEX HNS-11
STOCKERT GMBH
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