PMA P950018S003
- Device
- PERFLUORON (TM)
- Applicant
- Alcon Laboratories
- PMA number
- P950018
- Supplement
- S003
- Product code
- LWL
- Decision date
- 1999-10-12
- Classification
- Fluid, Intraocular
- Generic name
- Fluid, intraocular
- Approval order statement
- Approval for a manufacturing site located at Alcon Laboratories, Inc., 6201 South Freeway, Fort Worth, Texas 76134-2099.
Current openFDA PMA Record#
- Device
- PERFLUORON (TM)
- Applicant
- Alcon Laboratories
- PMA number
- P950018
- Supplement
- S003
- Product code
- LWL
- Generic name
- Fluid, intraocular
- Decision date
- 1999-10-12
- Decision code
- APPR
- Date received
- 1999-03-26
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Approval for a manufacturing site located at Alcon Laboratories, Inc., 6201 South Freeway, Fort Worth, Texas 76134-2099.