PMA P080014S023

Device
Cervista® HPV HR Assay
Applicant
Hologic, Inc.
PMA number
P080014
Supplement
S023
Product code
MAQ
Decision date
2018-10-09
Classification
Kit, Dna Detection, Human Papillomavirus
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Approval order statement
Transfer the purification and dilution operations for specified reagents within an existing manufacturing facility.
Summary
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Current openFDA PMA Record#

Device
Cervista® HPV HR Assay
Applicant
Hologic, Inc.
PMA number
P080014
Supplement
S023
Product code
MAQ
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Decision date
2018-10-09
Decision code
OK30
Date received
2018-09-10
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Transfer the purification and dilution operations for specified reagents within an existing manufacturing facility.