Atlas FDA

PREPSTAIN SYSTEM

FDA premarket approval P970018/S021 · decided 2010-06-30

Approval details

PMA number
P970018
Supplement
S021
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PREPSTAIN SYSTEM
Generic name
Processor, cervical cytology slide, automated
Applicant
Bd Diagnostic Systems
Date received
2010-04-05
Decision date
2010-06-30
Days to decision
86 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
APPROVAL FOR CHANGES MADE TO THE PREPSTAIN SOFTWARE TO REFLECT CUSTOMER PREFERENCE FOR ¿PREP ONLY¿ PROCESSING.

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510(k) clearances by this applicant

RecordFirmDate
BD BACTEC FXI Culture System (K260213)BD Diagnostic Systems2026-05-28
PASCO MIC AND MIC/ID PANELS, GEMIFLOXACIN (STREP) (K032518)Bd Diagnostic Systems2003-09-15
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM CEFOTAXIME 0.5-64 UG/ML (K032153)Bd Diagnostic Systems2003-09-11
PASCO MIC AND MIC/ID PANELS (K032259)Bd Diagnostic Systems2003-08-19
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-MEROPENEM 0.25-16 UG/ML (K031429)Bd Diagnostic Systems2003-06-06
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - NORFLOXACIN 0.25 - 16 UG/ML (K030091)Bd Diagnostic Systems2003-02-28