FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lipoprotein, Low Density, Removal

PMA: P910018 · Supplement: S021 · Decision Oct 14, 2016
Classifications
1
FEI Numbers
5
Registration Numbers
5

Basic Information

Device Name
Lipoprotein, Low Density, Removal
Trade Name
LIPOSORBER(R) LA-15 SYSTEM
PMA Number
P910018
Supplement Number
S021
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
October 14, 2016
Date Received
July 29, 2016
Supplement Type
Normal 180 Day Track
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for modifications to the instructions for use, operator's manual, and the patient guide for the LIPOSORBER® LA-15 System for familial hypercholesterolemia and integration of instructions for use for the LIPOSORBER® LA-15 System for familial hypercholesterolemia and focal segmental glomerulosclerosis.

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