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VITROS Immunodiagnostic Products Anti-HBe Reagent Pack and Calibrator

FDA premarket approval P100001/S015 · decided 2018-12-17

Approval details

PMA number
P100001
Supplement
S015
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VITROS Immunodiagnostic Products Anti-HBe Reagent Pack and Calibrator
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Ortho-Clinical Diagnostics
Date received
2018-10-16
Decision date
2018-12-17
Days to decision
62 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Rochester, NY
Statement
Approval for an additional manufacturing site located at NPA de México S.A. de C.V. dba Nypro, at Sor Juana Ines de la Cruz #20150, Parque Industrial Chilpancingo, 22509 Tijuana, Baja California, Mexico, limited to manufacturing of the Ortho-Clinical Diagnostics VITROS ECi/ECiQ Immunodiagnostic System

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