Atlas FDA

BD PREPSTAIN SYSTEM

FDA premarket approval P970018/S028 · decided 2014-04-28

Approval details

PMA number
P970018
Supplement
S028
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
BD PREPSTAIN SYSTEM
Generic name
Processor, cervical cytology slide, automated
Applicant
Bd Diagnostic Systems
Date received
2013-10-31
Decision date
2014-04-28
Days to decision
179 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
APPROVAL FOR THE BD PREPMATE¿ AUTOMATED ACCESSORY WITH THE UPGRADED CONTROL ELECTRONICS TO COMPLY WITH CURRENT TECHNOLOGIES.

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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