FDA 510(k) Applications Submitted by STOCKERT GMBH
| 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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