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

QUADROX-I, QUADROX-ID, QUADROX-IR OXYGENATORS

K Number: K132829 · Decision Oct 8, 2013
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
249
Applicant Total
44
Review Days
29

Basic Information

Device Name
QUADROX-I, QUADROX-ID, QUADROX-IR OXYGENATORS
K Number
K132829
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MAQUET CARDIOPULMONARY AG
Date Received
September 9, 2013
Decision Date
October 8, 2013
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

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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
K131666 ARTERIAL HLS CANNULA 13 FR NON-COATED, WITH BIOLINE COATING AND WITH SOFTLINE COATING
K130300 HEATER-COOLER UNIT HCU 40
K123288 HEMOCONCENTRATOR
K130639 ELITE-I (BI) DUAL LUMEN CATHETER; ELITE-I (RA) DUAL LUMEN CATHETER; ELITE-I (BIX)DUAL LUMEN CATHETER
Search all 44 clearances from MAQUET CARDIOPULMONARY AG →