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

Lipoprotein, Low Density, Removal

PMA: P910018 · Supplement: S040 · Decision Sep 26, 2024
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
S040
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
September 26, 2024
Date Received
August 30, 2024
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change in synthesis tank, timing of column bioburden reduction operation, and process automation including gel transfer operation, adjustment operation for gell filling volume, cap attachment operation, appearance inspection for final product release, transfer of intermediate products between processes.

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