PMA P950008S012
- Device
- SILICOM(TM) 1000 RETINALTAMPONADE
- Applicant
- Alcon
- PMA number
- P950008
- Supplement
- S012
- Product code
- LWL
- Decision date
- 2014-11-03
- Classification
- Fluid, Intraocular
- Generic name
- Fluid, intraocular
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT ALCON RESEARCH, LTD., IN FORT WORTH, TEXAS.
Current openFDA PMA Record#
- Device
- SILICOM(TM) 1000 RETINALTAMPONADE
- Applicant
- Alcon
- PMA number
- P950008
- Supplement
- S012
- Product code
- LWL
- Generic name
- Fluid, intraocular
- Decision date
- 2014-11-03
- Decision code
- APPR
- Date received
- 2014-07-07
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT ALCON RESEARCH, LTD., IN FORT WORTH, TEXAS.