FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BARD QUANTUM CVR
K Number: K962726
·
Decision Oct 30, 1996
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
33
Applicant Total
645
Review Days
107
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Basic Information
- Device Name
- BARD QUANTUM CVR
- K Number
- K962726
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4230
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- C.R. Bard, Inc.
- Date Received
- July 15, 1996
- Decision Date
- October 30, 1996
- Product Code
- DTP
- 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 |
|---|---|---|---|
| DTP | Defoamer, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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