FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure
K Number: K192838
·
Decision Apr 13, 2020
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
36
Applicant Total
15
Review Days
193
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Basic Information
- Device Name
- Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure
- K Number
- K192838
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4380
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Spectrum Medical , Ltd.
- Date Received
- October 3, 2019
- Decision Date
- April 13, 2020
- Product Code
- DWA
- 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 |
|---|---|---|---|
| DWA | Control, Pump Speed, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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