Atlas FDA

THINPREP 2000 SYSTEM

FDA premarket approval P950039/S012 · decided 2005-08-05

Approval details

PMA number
P950039
Supplement
S012
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
THINPREP 2000 SYSTEM
Generic name
Processor, cervical cytology slide, automated
Applicant
Hologic, Inc.
Date received
2004-08-10
Decision date
2005-08-05
Days to decision
360 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Malborough, MA
Statement
APPROVAL FOR AN ADDITION TO THE CURRENT LABELING, WITH REGARD TO THE EVALUATION OF GLANDULAR ABNORMALITIES USING THE THINPREP 2000 SYSTEM.

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