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AcrySof Posterior Chamber Intraocular Lenses and Delivery Systems

FDA premarket approval P930014/S152 · decided 2025-06-18

Approval details

PMA number
P930014
Supplement
S152
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AcrySof Posterior Chamber Intraocular Lenses and Delivery Systems
Generic name
intraocular lens
Applicant
Alcon Laboratories, Inc.
Date received
2024-12-10
Decision date
2025-06-18
Days to decision
190 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
approval for a manufacturing site located at [Alcon Huntington West Virginia, 2 Vision Lane, Lesage, West Virginia 25537 for manufacturing processes starting with injection molding and progressing through primary packaging and seal integrity testing.

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510(k) clearances by this applicant

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