FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lipoprotein, Low Density, Removal

PMA: P940016 · Supplement: S016 · Decision Aug 11, 2015
Classifications
1
FEI Numbers
5
Registration Numbers
5

Basic Information

Device Name
Lipoprotein, Low Density, Removal
Trade Name
H.E.L.P. PLASMAT FUTURA SYSTEM
PMA Number
P940016
Supplement Number
S016
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
August 11, 2015
Date Received
September 13, 2013
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE H.E.L.P. OPTIMIZED THERAPY (HOT) CONFIGURATION

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