FDA 510(k), K062251, REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804
FDA 510(k), K062251, REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804
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510(K) Number: K062251
Device Name: REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804
Manufacturer:
Device Classification Name: Catheter, Electrode Recording, Or Probe, Electrode Recording
Regulation Number: 870.1220
Classification Product Code: DRF
Date Received: 08/03/2006
Decision Date: 10/20/2006
Regulation Medical Specialty: Cardiovascular
Device Name: REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804
Manufacturer:
Device Classification Name: Catheter, Electrode Recording, Or Probe, Electrode Recording
Regulation Number: 870.1220
Classification Product Code: DRF
Date Received: 08/03/2006
Decision Date: 10/20/2006
Regulation Medical Specialty: Cardiovascular