FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Laser, Photodynamic Therapy

PMA: P990019 · Supplement: S007 · Decision Jul 7, 2011
Classifications
1
FEI Numbers
7
Registration Numbers
7

Basic Information

Device Name
System, Laser, Photodynamic Therapy
Trade Name
BLU-U BLUE LIGHT PHOTODYNAMIC THERAPY ILLUMINATOR
PMA Number
P990019
Supplement Number
S007
Device Class
FDA Class 3
Product Code
MVF
Generic Name
SYSTEM, LASER, PHOTODYNAMIC THERAPY
Medical Specialty
Unknown
Advisory Committee
General, Plastic Surgery
Decision
Approved
Decision Code
APPR
Decision Date
July 7, 2011
Date Received
June 27, 2011
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A SOFTWARE CHANGE TO ELIMINATE THE NEED TO ARTIFICIALLY LIMIT THE CYCLE LIFETIME FOR THE BLU-U TREATMENT LAMP SYSTEM.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MVF System, Laser, Photodynamic Therapy