Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon Toric Aspheric Hydrophobic Acrylic Intraocular Lens
FDA premarket approval P190018/S031 · decided 2024-05-29
Approval details
- PMA number
- P190018
- Supplement
- S031
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon Toric Aspheric Hydrophobic Acrylic Intraocular Lens
- Generic name
- intraocular lens
- Applicant
- Alcon Laboratories, LLC
- Date received
- 2023-12-07
- Decision date
- 2024-05-29
- Days to decision
- 174 days
- Decision code
- APPR
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Fort Worth, TX
- Statement
- approval for a new Gas Chromatography (GC) ratio instrument method for AcrySof® & Clareon® Intraocular Lenses
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