PMA P820060S004
- Device
- ABBOTT AFP-EIA DIAGNOSTIC KIT FOR NTDS
- Applicant
- Abbott Laboratories
- PMA number
- P820060
- Supplement
- S004
- Product code
- LOJ
- Decision date
- 1989-05-09
- Generic name
- KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER
Current openFDA PMA Record
- Device
- ABBOTT AFP-EIA DIAGNOSTIC KIT FOR NTDS
- Applicant
- Abbott Laboratories
- PMA number
- P820060
- Supplement
- S004
- Product code
- LOJ
- Generic name
- KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER
- Decision date
- 1989-05-09
- Decision code
- APPR
- Date received
- 1988-12-12
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material