FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Lens

PMA: P830033 · Supplement: S027 · Decision Jan 29, 1996
Classifications
1
FEI Numbers
59
Registration Numbers
59

Basic Information

Device Name
Intraocular Lens
Trade Name
SINGLE-PIECE AND THREE PIECE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENSES (IOLS)
PMA Number
P830033
Supplement Number
S027
Device Class
FDA Class 3
Product Code
HQL
Generic Name
intraocular lens
Regulation Number
886.3600
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
January 29, 1996
Date Received
July 28, 1994
Supplement Type
Normal 180 Day Track
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL TO CHANGE VENDORS OF THE POLYMETHYLMETHACRYLATE (PMMA) MATERIAL USED TO MANUFACTURE IOLS APROVED UNDER THIS PMA AND ITS SUPPLEMENTS

Classifications

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

Product Code Device Name
HQL Intraocular Lens