FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
K Number: K071572
·
Decision Jul 23, 2007
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
253
Applicant Total
21
Review Days
45
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Basic Information
- Device Name
- CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
- K Number
- K071572
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4350
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Terumo Corp.
- Date Received
- June 8, 2007
- Decision Date
- July 23, 2007
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| DTZ | Oxygenator, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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|---|---|---|---|
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