FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Lipoprotein, Low Density, Removal
PMA: P910018
·
Supplement: S011
·
Decision Jun 27, 2007
Classifications
1
FEI Numbers
5
Registration Numbers
5
Basic Information
- Device Name
- Lipoprotein, Low Density, Removal
- Trade Name
- LIPOSORBER LA-15 SYSTEM
- PMA Number
- P910018
- Supplement Number
- S011
- Device Class
- FDA Class 3
- Product Code
- MMY
- Generic Name
- Lipoprotein, low density, removal
- Medical Specialty
- Unknown
- Advisory Committee
- Gastroenterology, Urology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 27, 2007
- Date Received
- April 20, 2006
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO USE THE SULFLUX KP-05 PLASMA SEPARATOR AS A COMPONENT OF THE LIPOSORBER LA-15 SYSTEM.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MMY | Lipoprotein, Low Density, Removal | FDA class 3 | Unknown |