Atlas FDA

MONOPREP PAP TEST

FDA premarket approval P040052/S008 · decided 2008-10-16

Approval details

PMA number
P040052
Supplement
S008
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MONOPREP PAP TEST
Generic name
Processor, cervical cytology slide, automated
Applicant
Hologic, Inc.
Date received
2008-09-24
Decision date
2008-10-16
Days to decision
22 days
Decision code
OK30
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Malborough, MA
Statement
NEW SUPPLIER FOR THE MEMBRANE COMPONENT OF THE MPPT FILTER.

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