PMA P820060S007
- Device
- ABBOTT AFP-EIA LABELING CHANGE
- Applicant
- Abbott Laboratories
- PMA number
- P820060
- Supplement
- S007
- Product code
- LOJ
- Decision date
- 1993-05-13
- Generic name
- KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER
Current openFDA PMA Record#
- Device
- ABBOTT AFP-EIA LABELING CHANGE
- Applicant
- Abbott Laboratories
- PMA number
- P820060
- Supplement
- S007
- Product code
- LOJ
- Generic name
- KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER
- Decision date
- 1993-05-13
- Decision code
- APPR
- Date received
- 1993-03-09
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename