FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIO-CONSOLE 560

K Number: K080824 · Decision May 7, 2008
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
36
Applicant Total
29
Review Days
44

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Basic Information

Device Name
BIO-CONSOLE 560
K Number
K080824
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4380
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Perfusion Systems
Date Received
March 24, 2008
Decision Date
May 7, 2008
Product Code
DWA
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWA Control, Pump Speed, Cardiopulmonary Bypass

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Other Clearances by Medtronic Perfusion Systems

K Number Device Name
K240666 Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface (BB811); Affinity Fusion Oxygenator with Integrated Arterial Filter and Cardiotomy/Venous Reservoir with Balance Biosurface (BB841); Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface NON STERILE (BB811-NS)
K181954 autoLog IQ Autotransfusion System
K123351 AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACE
K101186 AFFINITY VARD SUB-ASSEMBLY FOR CPS (CARMEDA COATED), PURGELINE (UNCOATED), HOLDING BAG
K090869 MIRCSP (MINIMALLY INVASIVE RETROGRADE CORONARY SINUS PERFUSION) MANUAL INFLATE CANNULA, MODEL 94113TD
K061254 EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222
K052524 BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT
K052372 MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C
K051303 BIO-CONSOLE, MODEL 560
K051040 HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR
Search all 29 clearances from Medtronic Perfusion Systems →