SILIKON 1000
FDA premarket approval P950008/S003 · decided 2002-01-23
Approval details
- PMA number
- P950008
- Supplement
- S003
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- SILIKON 1000
- Generic name
- Fluid, intraocular
- Applicant
- Alcon
- Date received
- 2001-10-04
- Decision date
- 2002-01-23
- Days to decision
- 111 days
- Decision code
- APPR
- Product code
- LWL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Fort Worth, TX
- Statement
- APPROVAL FOR MODIFICATION OF THE MOLECULAR WEIGHT RANGE SPECIFICATION FOR SILIKON 1000 FROM 36,000 - 48,000 DALTON TO 32,850 - 47,000 DALTON.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| ALCON VISION SYSTEM (K063583) | Alcon | 2008-05-09 |
| OPTI-FREE EXPRESS MULTI-PURPOSE SOLUTION (K981574) | Alcon | 1998-07-06 |