CLARISERT PRELOADED IOL SYSTEM
FDA premarket approval P080004/S016 · decided 2017-03-31
Approval details
- PMA number
- P080004
- Supplement
- S016
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- CLARISERT PRELOADED IOL SYSTEM
- Generic name
- intraocular lens
- Applicant
- Hoya Surgical Optics, Inc.
- Date received
- 2016-12-28
- Decision date
- 2017-03-31
- Days to decision
- 93 days
- Decision code
- APPR
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Chino Hills, CA
- Statement
- Approval for changes in the spherical aberration and thickness of the optic lens for your iSert® IOLs. You also requested approval for this lens to be distributed under a new private label under Bausch + Lomb Inc. as the ClarisertTM Preloaded IOL System (Model CLSRT).
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| HOYA IS INJECTOR SYSTEM (K081346) | Hoya Surgical Optics, Inc. | 2009-03-23 |