FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Lens

PMA: P860059 · Supplement: S076 · Decision Sep 17, 1996
Classifications
1
FEI Numbers
59
Registration Numbers
59

Basic Information

Device Name
Intraocular Lens
Trade Name
TIER A LENS MODELS UPB360GN AND UP320F
PMA Number
P860059
Supplement Number
S076
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
September 17, 1996
Date Received
April 5, 1996
Supplement Type
Normal 180 Day Track
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL OF MODELS UPB360GN AND UP320F AS TIER A MODIFICATIONS OF PREVIOUSLY APPROVED PARENT IOLS. MODEL UPB360GN WILL BE MARKETED UNDER THE TRADE NAME TOP NOTCH

Classifications

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

Product Code Device Name
HQL Intraocular Lens