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AFP IMMULITE SUBSTRATE REAGENT

FDA premarket approval P010007/S008 · decided 2012-04-05

Approval details

PMA number
P010007
Supplement
S008
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AFP IMMULITE SUBSTRATE REAGENT
Generic name
KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
Applicant
Siemens Healthcare Diagnostics, Inc.
Date received
2011-12-19
Decision date
2012-04-05
Days to decision
108 days
Decision code
APPR
Product code
LOK
Advisory committee
Immunology
Expedited review
No
Location
Tarrytown, NY
Statement
APPROVAL FOR A CHANGE TO REMOVE THE SLIP AGENT FROM THE BOTTLE USED TO PACKAGE THE IMMULITE SUBSTRATE.

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