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

CAPIOX CARDIOTOMY RESERVOIR

K Number: K030505 · Decision May 14, 2003
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
134
Applicant Total
43
Review Days
84

Basic Information

Device Name
CAPIOX CARDIOTOMY RESERVOIR
K Number
K030505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Date Received
February 19, 2003
Decision Date
May 14, 2003
Product Code
DPW
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
DPW Flowmeter, Blood, Cardiovascular

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Other Clearances by TERUMO CARDIOVASCULAR SYSTEMS CORP.

K Number Device Name
K153140 Terumo Capiox SX18 Oxygenator/ Hardshell Reservoir, Terumo Capiox SX18 Oxygenator/ Hardshell Reservoir with Xcoating, Terumo Capiox SX25 Oxygenator/Hardshell Reservoir, Terumo Capiox SX25 Oxygenator/Hardshell Reservoir with Xcoating
K133658 CDI BLOOD PARAMETER MONITORING SYSTEM 500
K131041 ADVANCED PERFUSION SYSTEM 1
K132451 SARNS SOFT-FLOW AORTIC CANNULA
K133151 SARNS HIGH FLOW AORTIC ARCH CANNULA
K130359 CAPIOX SX18 HOLLOW FIBER OXYGENATOR WITH DETACHABLE HARDSHELL RESERVOIR, CAPIOX SX25 HOLLOW FIBER OXGENATOR WITH DETACHA
K130333 CAPIX RX HOLLOW FIBER OXYGENATOR WITH/WITHOUT HARDSHELL RESERVOIR
K123039 CDI BLOOD PARAMETER MONITORING SYSTEM 500
K113214 TLINK DATA MANAGEMENT SYSTEM (DMS)
K112587 ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR,
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