FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Lipoprotein, Low Density, Removal

PMA: P910018 · Supplement: S028 · Decision Dec 22, 2020
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
S028
Device Class
FDA Class 3
Product Code
MMY
Generic Name
Lipoprotein, low density, removal
Medical Specialty
Unknown
Advisory Committee
Gastroenterology, Urology
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
December 22, 2020
Date Received
November 27, 2020
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change in the sterilization bag supplier for the SULFLUX KP-05 Plasma Separator for 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
MMY Lipoprotein, Low Density, Removal