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Atellica IM Alpha Fetoprotien (AFP) Assay

FDA premarket approval P930036/S014 · decided 2020-04-03

Approval details

PMA number
P930036
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Atellica IM Alpha Fetoprotien (AFP) Assay
Generic name
KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
Applicant
Siemens Healthcare Diagnostics, Inc.
Date received
2020-03-09
Decision date
2020-04-03
Days to decision
25 days
Decision code
OK30
Product code
LOK
Advisory committee
Immunology
Expedited review
No
Location
East Walpole, MA
Statement
Modification to the manufacturing process to add a second manufacturing site for optional sample handling subsystem (Atellica Direct Load) for the Atellica IM Analyzer (Immunoassay Module).

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