Atlas FDA

BD FocalPoint GS Imaging System

FDA premarket approval P950009/S026 · decided 2022-07-11

Approval details

PMA number
P950009
Supplement
S026
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BD FocalPoint GS Imaging System
Generic name
READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED
Applicant
Bd Diagnostics
Date received
2022-06-15
Decision date
2022-07-11
Days to decision
26 days
Decision code
OK30
Product code
MNM
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
Change of supplier for an instrument component.

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