Atlas FDA

BD FOCALPOINT SYSTEM

FDA premarket approval P950009/S009 · decided 2009-07-24

Approval details

PMA number
P950009
Supplement
S009
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
BD FOCALPOINT SYSTEM
Generic name
READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED
Applicant
Bd Diagnostics
Date received
2009-03-26
Decision date
2009-07-24
Days to decision
120 days
Decision code
APPR
Product code
MNM
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
APPROVAL FOR DESIGN CHANGES TO THE IMAGE, CAPTURE AND FOCUS (ICF) CIRCUIT BOARD IN THE BD FOCALPOINT PROFILER.

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