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

SORIN C5 SYSTEM MODEL 58-00-00

K Number: K093882 · Decision Jan 15, 2010
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
51
Applicant Total
20
Review Days
28

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Basic Information

Device Name
SORIN C5 SYSTEM MODEL 58-00-00
K Number
K093882
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sorin Group Deutschland GmbH
Date Received
December 18, 2009
Decision Date
January 15, 2010
Product Code
DTQ
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
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

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K Number Device Name
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K112225 SORIN CENTRIFUGAL PUMP 5 (CP5)
K103468 STOCKERT CENTRIFUGAL PUMP (SCP PLUS) (COMPLETE) OR (FOR S5/C5 SYSTEMS)
K103762 SORIN C5 SYSTEM; 85/C5 MAST ROLLER PUMP SYSTEM 150(1X RP 150 AND CONTROL PANEL WITH CONNECTING CABLES); S5/C5 MAST ROLLE
K103469 STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05
K103168 B-CARE5 (B-CARE5 SENSOR MODULE, VENOUS SENSOR, HOLDER FOR MEASURING HEAD)
K101046 STOCKERT S5 SYSTEM AND GAS BLENDER AND SORIN C5 SYSTEM
Search all 20 clearances from Sorin Group Deutschland GmbH →