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CERVISTA HPV 16/18

FDA premarket approval P080015/S011 · decided 2013-12-03

Approval details

PMA number
P080015
Supplement
S011
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CERVISTA HPV 16/18
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Applicant
Hologic, Inc.
Date received
2013-11-08
Decision date
2013-12-03
Days to decision
25 days
Decision code
OK30
Product code
MAQ
Advisory committee
Microbiology
Expedited review
No
Location
Malborough, MA
Statement
INCREASE OF THE MANUFACTURING LOT SIZE FOR THE CLEAVASE ENZYME SOLUTION USING MANUAL FILLING WITH GRAVIMETRIC CONFIRMATION.

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