PMA P020050S024
- Device
- ALLEGRETTO WAVE EYE-Q
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P020050
- Supplement
- S024
- Product code
- LZS
- Decision date
- 2015-10-15
- Classification
- Excimer Laser System
- Generic name
- Excimer laser system
- Approval order statement
- APPROVAL FOR LABELING REVISIONS TO ADDRESS DESIGN CHANGE.
Current openFDA PMA Record#
- Device
- ALLEGRETTO WAVE EYE-Q
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P020050
- Supplement
- S024
- Product code
- LZS
- Generic name
- Excimer laser system
- Decision date
- 2015-10-15
- Decision code
- APPR
- Date received
- 2015-07-29
- Supplement type
- Real-Time Process
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Approval order statement
- APPROVAL FOR LABELING REVISIONS TO ADDRESS DESIGN CHANGE.