PMA P950008S006
- Device
- SILIKON 1000
- Applicant
- Alcon
- PMA number
- P950008
- Supplement
- S006
- Product code
- LWL
- Decision date
- 2003-12-22
- Classification
- Fluid, Intraocular
- Generic name
- Fluid, intraocular
- Approval order statement
- APPROVAL FOR A CHANGE TO THE SPECIFICATION FOR THE FINISHED PRODUCT VISCOSITY RANGE, I.E., FROM THE RANGE OF 900 TO 1200 CS TO THE RANG OF 900 TO 1250 CS.
Current openFDA PMA Record#
- Device
- SILIKON 1000
- Applicant
- Alcon
- PMA number
- P950008
- Supplement
- S006
- Product code
- LWL
- Generic name
- Fluid, intraocular
- Decision date
- 2003-12-22
- Decision code
- APPR
- Date received
- 2003-12-15
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR A CHANGE TO THE SPECIFICATION FOR THE FINISHED PRODUCT VISCOSITY RANGE, I.E., FROM THE RANGE OF 900 TO 1200 CS TO THE RANG OF 900 TO 1250 CS.