FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CAPIOX 308 HOLLOW FIBER OXYGENATOR W/INTEGRATED HEAT EXCHANGE
K Number: K961734
·
Decision Jul 7, 1997
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
253
Applicant Total
143
Review Days
430
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Basic Information
- Device Name
- CAPIOX 308 HOLLOW FIBER OXYGENATOR W/INTEGRATED HEAT EXCHANGE
- K Number
- K961734
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4350
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Terumo Medical Corp.
- Date Received
- May 3, 1996
- Decision Date
- July 7, 1997
- 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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