Atlas FDA

THINPREP IMAGING SYSTEM

FDA premarket approval P020002/S007 · decided 2014-04-29

Approval details

PMA number
P020002
Supplement
S007
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
THINPREP IMAGING SYSTEM
Generic name
READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED
Applicant
Hologic, Inc.
Date received
2014-01-30
Decision date
2014-04-29
Days to decision
89 days
Decision code
APPR
Product code
MNM
Advisory committee
Pathology
Expedited review
No
Location
Malborough, MA
Statement
APPROVAL FOR THE INTRODUCTION OF THE THINPREP® IMAGER DUO IMAGING STATION, HARDWARE (CAMERA AND EXTERIOR HOUSING) CHANGES, AND ASSOCIATED SOFTWARE CHANGES.

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