Atlas FDA

MONOPREP PAP TEST

FDA premarket approval P040052/S005 · decided 2008-08-11

Approval details

PMA number
P040052
Supplement
S005
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Express GMP Supplement
Trade name
MONOPREP PAP TEST
Generic name
Processor, cervical cytology slide, automated
Applicant
Hologic, Inc.
Date received
2007-10-22
Decision date
2008-08-11
Days to decision
294 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Malborough, MA
Statement
APPROVAL FOR MANUFACTURING SITES LOCATED IN LINCOLNSHIRE, ILLINOIS AND WAUKEGAN, ILLINOIS.

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