Atlas FDA

ACRYSOF RESTOR INTRAOCULAR LENSES

FDA premarket approval P040020/S047 · decided 2013-05-21

Approval details

PMA number
P040020
Supplement
S047
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ACRYSOF RESTOR INTRAOCULAR LENSES
Generic name
Lens, multifocal intraocular
Applicant
Alcon Research, Ltd.
Date received
2013-04-22
Decision date
2013-05-21
Days to decision
29 days
Decision code
OK30
Product code
MFK
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
RELOCATE PACKAGING AND LABELING EQUIPMENT.

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