PMA P090022S010
- Device
- SOFTEC HD POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Lenstec, Inc.
- PMA number
- P090022
- Supplement
- S010
- Product code
- HQL
- Decision date
- 2012-05-11
- Generic name
- intraocular lens
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED IN PETERSBURG, FLORIDA.
Current openFDA PMA Record#
- Device
- SOFTEC HD POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Lenstec, Inc.
- PMA number
- P090022
- Supplement
- S010
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2012-05-11
- Decision code
- APPR
- Date received
- 2011-11-02
- 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 LOCATED IN PETERSBURG, FLORIDA.