FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
B-Capta
K Number: K202154
·
Decision Apr 1, 2021
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
46
Applicant Total
7
Review Days
241
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Basic Information
- Device Name
- B-Capta
- K Number
- K202154
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4330
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Livanova Deutschland, GmbH
- Date Received
- August 3, 2020
- Decision Date
- April 1, 2021
- Product Code
- DRY
- 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 |
|---|---|---|---|
| DRY | Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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