FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

QUADROX-I ADULT WITH AND WITHOUT INTEGRATED ARTERIAL FILTER WITH SOFTLINE COATING, MODEL# HMO 70000, HMO 71000

K Number: K082117 · Decision Feb 18, 2009
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
253
Applicant Total
44
Review Days
205

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Basic Information

Device Name
QUADROX-I ADULT WITH AND WITHOUT INTEGRATED ARTERIAL FILTER WITH SOFTLINE COATING, MODEL# HMO 70000, HMO 71000
K Number
K082117
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Maquet Cardiopulmonary, AG
Date Received
July 28, 2008
Decision Date
February 18, 2009
Product Code
DTZ
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
DTZ Oxygenator, Cardiopulmonary Bypass

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTZ), ordered by most recent decision date.

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Other Clearances by Maquet Cardiopulmonary, AG

K Number Device Name
K150267 QUADROX-i Adult/Small Adult Oxygenators;QUADROX-iD Adult Oxygenators
K140569 ANTEGRADE CARDIOPLEGIA CANNULA(N-TYPE)
K141432 NEONATAL VENOUS HARDSHELL CARDIOTOMY RESERVIOR, PEDIATRIC VENOUS HARDSHELL CARDIOTOMY RESERVIOR, NEONATAL VENOUS HARDHSH
K133598 CARDIOHELP SYSTEM
K133265 QUADROX-IR ADULT AND SMALL ADULT
K132166 VENOUS HARDSHELL CARDIOTOMY RESERVOIR; NON-COATED, NON-TIGHT/ VACUUM-TIGHT/ WITH SOFTLINE COATING, VACUUM-TIGHT
K132829 QUADROX-I, QUADROX-ID, QUADROX-IR OXYGENATORS
K131666 ARTERIAL HLS CANNULA 13 FR NON-COATED, WITH BIOLINE COATING AND WITH SOFTLINE COATING
K130300 HEATER-COOLER UNIT HCU 40
K123288 HEMOCONCENTRATOR
Search all 44 clearances from Maquet Cardiopulmonary, AG →