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AcrySof Posterior Chamber Intraocular Lens

FDA premarket approval P930014/S138 · decided 2022-10-28

Approval details

PMA number
P930014
Supplement
S138
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AcrySof Posterior Chamber Intraocular Lens
Generic name
intraocular lens
Applicant
Alcon Laboratories, Inc.
Date received
2021-07-01
Decision date
2022-10-28
Days to decision
484 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Approval for an updated analytical testing method for determination of Ethylene Oxide (EO) sterilant residuals and residual acetone on the subject devices by headspace gas chromatography.

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