PERFLUORON
FDA premarket approval P950018/S011 · decided 2013-08-14
Approval details
- PMA number
- P950018
- Supplement
- S011
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- PERFLUORON
- Generic name
- Fluid, intraocular
- Applicant
- Alcon Laboratories
- Date received
- 2009-07-14
- Decision date
- 2013-08-14
- Days to decision
- 1492 days
- Decision code
- APPR
- Product code
- LWL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Fort Worth, TX
- Statement
- APPROVAL FOR A MODIFIED STABILITY PROTOCOL, A CHANGE IN THE PACKAGING TO AN ALTERNATE ALUMINUM SEAL WITH A FLIP-OFF CAP, AND THE ADDITION OF A PRE-PROCESSING MODIFICATION TO SILICONIZE THE STOPPERS USED IN THE FILLING, STOPPING, AND SEALING OF PERFLUORON..
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| NEXT GENERATION LASER (K062624) | Alcon Laboratories | 2007-11-05 |
| SMALL VOLUME SYRINGE (K062865) | Alcon Laboratories | 2007-08-23 |
| RGP MULTI-PURPOSE SOLUTION ID 100136 (K000148) | Alcon Laboratories | 2000-04-11 |
| OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP (K984573) | Alcon Laboratories | 1999-09-16 |
| OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER (K990480) | Alcon Laboratories | 1999-05-10 |
| MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 (K984575) | Alcon Laboratories | 1999-01-14 |
| OPTI-ONE MULTI-PURPOSE SOLUTION (K983973) | Alcon Laboratories | 1998-12-18 |
| MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 (K983780) | Alcon Laboratories | 1998-12-18 |