Device, Iontophoresis, Other Uses
Hidrex Gmbh's record for this product code
MDR events0All time
Recalls3All time
510(k) clearances1All time
Recent MDR events
0 adverse event reports on file
No MDR events on file for Hidrex Gmbh under this product code.
Recalls
3 recall events for this product code
- TerminatedFeb 22, 2017
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
View FDA record ↗ - TerminatedFeb 22, 2017
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
View FDA record ↗ - TerminatedFeb 22, 2017
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
View FDA record ↗
510(k) clearances
1 clearances for this product code