PMA P980031S006
- Device
- INTACS PRESCRIPTION INSERTS
- Applicant
- Addition Technology
- PMA number
- P980031
- Supplement
- S006
- Product code
- LQE
- Decision date
- 2003-11-05
- Classification
- Implant, Corneal, Refractive
- Generic name
- Implant, corneal, refractive
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE IN SUNNYVALE, CALIFORNIA.
Current openFDA PMA Record#
- Device
- INTACS PRESCRIPTION INSERTS
- Applicant
- Addition Technology
- PMA number
- P980031
- Supplement
- S006
- Product code
- LQE
- Generic name
- Implant, corneal, refractive
- Decision date
- 2003-11-05
- Decision code
- APPR
- Date received
- 2003-05-14
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE IN SUNNYVALE, CALIFORNIA.