PMA P810025S025
- Device
- AMVISC AND AMVISC PLUS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P810025
- Supplement
- S025
- Product code
- LZP
- Decision date
- 2006-03-14
- Generic name
- AID, SURGICAL, VISCOELASTIC
- Approval order statement
- REMOVAL OF THE CHLOROFORM TREATMENT STEP FROM THE MANUFACTURING PROCESS FOR THE AMVISC AND AMVISC PLUS.
Current openFDA PMA Record#
- Device
- AMVISC AND AMVISC PLUS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P810025
- Supplement
- S025
- Product code
- LZP
- Generic name
- AID, SURGICAL, VISCOELASTIC
- Decision date
- 2006-03-14
- Decision code
- OK30
- Date received
- 2006-02-17
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- REMOVAL OF THE CHLOROFORM TREATMENT STEP FROM THE MANUFACTURING PROCESS FOR THE AMVISC AND AMVISC PLUS.