PMA P840039S052
- Device
- BIOBURDEN TESTING
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P840039
- Supplement
- S052
- Product code
- HQL
- Decision date
- 2003-07-23
- Classification
- Intraocular Lens
- Generic name
- intraocular lens
- Approval order statement
- CHANGE IN THE FREQUENCY OF THE BIOBURDEN TESTING.
Current openFDA PMA Record#
- Device
- BIOBURDEN TESTING
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P840039
- Supplement
- S052
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2003-07-23
- Decision code
- OK30
- Date received
- 2003-06-23
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE IN THE FREQUENCY OF THE BIOBURDEN TESTING.