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

CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR

K Number: K130280 · Decision Mar 13, 2013
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
249
Applicant Total
4
Review Days
36

Basic Information

Device Name
CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR
K Number
K130280
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TERUMO Corporation
Date Received
February 5, 2013
Decision Date
March 13, 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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K Number Device Name
K130493 CAPIOX RX05 HOLLOW FIBER OXYGENATOR/RESERVOIR
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K113335 HEARTRAIL III GUIDING CATHETER