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ADVIA Centaur Anti-HBe2 (AHBe2) Assay

FDA premarket approval P200017/S001 · decided 2022-01-06

Approval details

PMA number
P200017
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ADVIA Centaur Anti-HBe2 (AHBe2) Assay
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Siemens Healthcare Diagnostics, Inc.
Date received
2021-08-10
Decision date
2022-01-06
Days to decision
149 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Tarrytown, NY
Statement
Approval for migration of the ADVIA Centaur Anti-HBe2 (aHBe2) assay to the Atellica IM analyzer. The device, as modified, will be marketed under the trade name Atellica IM Anti-HBe2 (aHBe2).

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