PMA P950018S005
- Device
- PERFLUORON
- Applicant
- Alcon Laboratories
- PMA number
- P950018
- Supplement
- S005
- Product code
- LWL
- Decision date
- 2001-03-27
- Classification
- Fluid, Intraocular
- Generic name
- Fluid, intraocular
- Approval order statement
- TO ELIMINATE THE WATER CONTENT TESTING AND THE ODOR CHECK ON THE PERFLUORO-N-OCTANE RAW MATERIAL.
Current openFDA PMA Record#
- Device
- PERFLUORON
- Applicant
- Alcon Laboratories
- PMA number
- P950018
- Supplement
- S005
- Product code
- LWL
- Generic name
- Fluid, intraocular
- Decision date
- 2001-03-27
- Decision code
- OK30
- Date received
- 2001-02-26
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- TO ELIMINATE THE WATER CONTENT TESTING AND THE ODOR CHECK ON THE PERFLUORO-N-OCTANE RAW MATERIAL.