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ADVIA CENTAUR IMMUNOASSAY

FDA premarket approval P930036/S007 · decided 2017-04-26

Approval details

PMA number
P930036
Supplement
S007
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ADVIA CENTAUR IMMUNOASSAY
Generic name
KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
Applicant
Siemens Healthcare Diagnostics, Inc.
Date received
2016-10-20
Decision date
2017-04-26
Days to decision
188 days
Decision code
APPR
Product code
LOK
Advisory committee
Immunology
Expedited review
No
Location
East Walpole, MA
Statement
Approval for wetcake manufacturing process changes to the ADVIA Centaur AFP Solid Phase reagent to achieve the current hook specification of >1,000 ng/mL with an AFP containing sample that is between 1,000,000 to 1,150,000 ng/mL.

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