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CERVISTA HPV HR

FDA premarket approval P080014/S004 · decided 2010-10-26

Approval details

PMA number
P080014
Supplement
S004
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CERVISTA HPV HR
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Applicant
Hologic, Inc.
Date received
2010-10-05
Decision date
2010-10-26
Days to decision
21 days
Decision code
OK30
Product code
MAQ
Advisory committee
Microbiology
Expedited review
No
Location
Marlborough, MA
Statement
CHANGES IN THE FILL VOLUME OF THE WASH BUFFER AND AN INCREASE IN SAMPLE SIZE OF THE INCOMING COMPONENTS BEING TESTED.

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