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ACRYSOF INTRAOCULAR LENS

FDA premarket approval P930014/S069 · decided 2014-04-28

Approval details

PMA number
P930014
Supplement
S069
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ACRYSOF INTRAOCULAR LENS
Generic name
intraocular lens
Applicant
Alcon Laboratories, Inc.
Date received
2013-07-31
Decision date
2014-04-28
Days to decision
271 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR THREE ALTERNATE POLYPROPYLENE MATERIALS, BASELL PD702, EXXON ACHIEVE 1605, AND EXXON PP1105E1, FOR INTRAOCULAR LENS (IOL) DEVICE PRIMARY PACKAGING.

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