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MONOPREP PAP TEST

FDA premarket approval P040052/S001 · decided 2007-12-14

Approval details

PMA number
P040052
Supplement
S001
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
MONOPREP PAP TEST
Generic name
Processor, cervical cytology slide, automated
Applicant
Hologic, Inc.
Date received
2006-05-03
Decision date
2007-12-14
Days to decision
590 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Malborough, MA
Statement
APPROVAL OF THE POST-APPROVAL STUDY.

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