FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CAPIOX SP PUMP WITH X-COATING PRODUCT CODE: CXSP45X
K Number: K012209
·
Decision Aug 15, 2001
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
83
Applicant Total
43
Review Days
30
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Basic Information
- Device Name
- CAPIOX SP PUMP WITH X-COATING PRODUCT CODE: CXSP45X
- K Number
- K012209
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.4360
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Terumo Cardiovascular Systems Corp.
- Date Received
- July 16, 2001
- Decision Date
- August 15, 2001
- Product Code
- KFM
- 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 |
|---|---|---|---|
| KFM | Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type | FDA class 2 | Cardiovascular |
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|---|---|---|---|
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| K123039 | CDI BLOOD PARAMETER MONITORING SYSTEM 500 | Nov 20, 2012 | Substantially Equivalent |
| K113214 | TLINK DATA MANAGEMENT SYSTEM (DMS) | Feb 7, 2012 | Substantially Equivalent |
| K112587 | ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR, | Dec 19, 2011 | Substantially Equivalent |