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IMMULITE/IMMULITE 1000/IMMULITE 2000/IMMULITE 2500 AFP

FDA premarket approval P010007/S004 · decided 2010-01-21

Approval details

PMA number
P010007
Supplement
S004
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
IMMULITE/IMMULITE 1000/IMMULITE 2000/IMMULITE 2500 AFP
Generic name
KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
Applicant
Siemens Healthcare Diagnostics, Inc.
Date received
2009-11-02
Decision date
2010-01-21
Days to decision
80 days
Decision code
APPR
Product code
LOK
Advisory committee
Immunology
Expedited review
No
Location
Tarrytown, NY
Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT SIEMENS HEALTHCARE DIAGNOSTICS IN NEWARK, DELAWARE.

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