FDA 510(k), K042616, BIOMEDIX PADNET LAB
FDA 510(k), K042616, BIOMEDIX PADNET LAB
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510(K) Number: K042616
Device Name: BIOMEDIX PADNET LAB
Manufacturer:
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: 870.2780
Classification Product Code: JOM
Date Received: 09/23/2004
Decision Date: 10/12/2004
Regulation Medical Specialty: Cardiovascular
Device Name: BIOMEDIX PADNET LAB
Manufacturer:
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: 870.2780
Classification Product Code: JOM
Date Received: 09/23/2004
Decision Date: 10/12/2004
Regulation Medical Specialty: Cardiovascular