Atlas FDA

AcrySof® IQ Aspheric IOL with the UltraSertTM Pre-loaded Delivery System AU00T0

FDA premarket approval P930014/S092 · decided 2016-10-12

Approval details

PMA number
P930014
Supplement
S092
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
AcrySof® IQ Aspheric IOL with the UltraSertTM Pre-loaded Delivery System AU00T0
Generic name
intraocular lens
Applicant
Alcon Laboratories, Inc.
Date received
2016-07-20
Decision date
2016-10-12
Days to decision
84 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Approval for modifications to your real time shelf life protocol to substitute the aerosol microbial challenge test with the microbial barrier test and to add a seal strength test for your AcrySof® IQ Aspheric IOL with the UltraSertTM Pre-Loaded Delivery System, Model AU00T0.

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