Atlas FDA

Cervista HPV HR Assay

FDA premarket approval P080014/S024 · decided 2018-11-15

Approval details

PMA number
P080014
Supplement
S024
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Cervista HPV HR Assay
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Applicant
Hologic, Inc.
Date received
2018-10-16
Decision date
2018-11-15
Days to decision
30 days
Decision code
OK30
Product code
MAQ
Advisory committee
Microbiology
Expedited review
No
Location
Marlborough, MA
Statement
Changes to manufacturing sites or vendors of critical raw materials.

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