Medical Device Manufacturer · DE , Freiburg

Stockert GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Recent clearances: STOCKERT NEURO N50, MODEL12267, MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098, STIMUPLEX PEN

5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Stockert GmbH Neurology ✕

1 devices
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