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Aptima HBV Quant Assay

FDA premarket approval P170025/S009 · decided 2019-03-21

Approval details

PMA number
P170025
Supplement
S009
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Aptima HBV Quant Assay
Generic name
Hepatitis Viral B DNA Detection
Applicant
Hologic, Inc.
Date received
2019-02-21
Decision date
2019-03-21
Days to decision
28 days
Decision code
OK30
Product code
MKT
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
Transfer Quality Control testing services for components and raw materials to a separate contractor facility.

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