AUTODELFIA / DELFIA XPRESS HAFP TEST SYSTEM
FDA premarket approval P970037/S006 · decided 2011-06-24
Approval details
- PMA number
- P970037
- Supplement
- S006
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- AUTODELFIA / DELFIA XPRESS HAFP TEST SYSTEM
- Generic name
- KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
- Applicant
- Revvity, Inc.
- Date received
- 2011-06-13
- Decision date
- 2011-06-24
- Days to decision
- 11 days
- Decision code
- OK30
- Product code
- LOK
- Advisory committee
- Immunology
- Expedited review
- No
- Location
- Waltham, MA
- Statement
- CHANGE IN THE TOPO (TRIOCTYLPHOSPHINE OXIDE) RAW MATERIAL TYPE USED IN THE MANUFACTURING OF THE DELFIA INDUCER.
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