FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Lens

PMA: P820035 · Supplement: S012 · Decision Dec 20, 1991
Classifications
1
FEI Numbers
59
Registration Numbers
59

Basic Information

Device Name
Intraocular Lens
Trade Name
ZIRCONIA SILICATE BEAD IOL TUMBLE POLISHING
PMA Number
P820035
Supplement Number
S012
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
December 20, 1991
Date Received
August 21, 1991
Supplement Type
Normal 180 Day Track
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Classifications

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

Product Code Device Name
HQL Intraocular Lens