Cable, Transducer And Electrode, Patient, (including Connector)
Philips North America Llc's record for this product code
MDR events2All time
Recalls1All time
510(k) clearances0All time
Recent MDR events
2 adverse event reports on file
Recalls
1 recall events for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Philips North America Llc under this product code.