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

SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800

K Number: K033641 · Decision Dec 11, 2003
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
43
Review Days
21

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Basic Information

Device Name
SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800
K Number
K033641
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cobe Cardiovascular, Inc.
Date Received
November 20, 2003
Decision Date
December 11, 2003
Product Code
DTN
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
DTN Reservoir, Blood, Cardiopulmonary Bypass

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Other Clearances by Cobe Cardiovascular, Inc.

K Number Device Name
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K040184 DIDECO MICRO 40 PH.I.S.I.O. ADULT ARTERIAL FILTER
K030462 COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC, MODEL 050300700
K021830 SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM
K011835 COBE REVOLUTION
K013480 COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR
K012763 SORIN BIOMEDICA SMART BCD VANGUARD,SURFACE MODIFIED BLOOD CARDIOPLEGIA SYSTEM
K001509 STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE
K012898 MODIFICATION TO: CSC14 BLOOD CARDIOPLEGIA SYSTEM
Search all 43 clearances from Cobe Cardiovascular, Inc. →