IMMULITE/IMMULITE 1000/IMMULITE 2000 AFP
FDA premarket approval P010007/S012 · decided 2020-08-18
Approval details
- PMA number
- P010007
- Supplement
- S012
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- IMMULITE/IMMULITE 1000/IMMULITE 2000 AFP
- Generic name
- KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
- Applicant
- Siemens Healthcare Diagnostics, Inc.
- Date received
- 2020-07-23
- Decision date
- 2020-08-18
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- LOK
- Advisory committee
- Immunology
- Expedited review
- No
- Location
- Tarrytown, NY
- Statement
- Removal of redundant annual stability testing.
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