PMA P120008S029
- Device
- ARCHITECT AFP / Alinity i AFP
- Applicant
- Abbott Laboratories
- PMA number
- P120008
- Supplement
- S029
- Product code
- LOK
- Decision date
- 2024-03-22
- Classification
- Immunology
- Generic name
- KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
- Approval order statement
- to change a component’s incoming (sponsor) specification
Current openFDA PMA Record#
- Device
- ARCHITECT AFP / Alinity i AFP
- Applicant
- Abbott Laboratories
- PMA number
- P120008
- Supplement
- S029
- Product code
- LOK
- Generic name
- KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
- Decision date
- 2024-03-22
- Decision code
- OK30
- Date received
- 2024-02-22
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- to change a component’s incoming (sponsor) specification