Atlas FDA

PREPSTAIN SYSTEM

FDA premarket approval P970018/S009 · decided 2005-02-11

Approval details

PMA number
P970018
Supplement
S009
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
2005-01-10
Decision date
2005-02-11
Days to decision
32 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
APPROVAL FOR MODIFICATION TO THE SUREPATH SLIDE PREPARATION METHOD WHICH WILL BE MARKETED UNDER THE TRADE NAME PREPSTAIN SYSTEM AND IS INDICATED FOR USE AS A LIQUID-BASED THIN LAYER CELL PREPARATION PROCESS. THE PRESTAIN SYSTEM PRODUCES SUREPATH SLIDES THAT ARE INTENDED AS REPLACEMENTS FOR CONVENTIONAL GYNECOLOGIC PAP SMEARS. SUREPATH SLIDES ARE INTENDED FOR USE IN THE SCREENING AND DETECTION OF CERVICAL CANCER, PRE-CANCEROUS LESIONS, ATYPICAL CELLS AND ALL OTHER CYTOLOGIC CATEGORIES AS DEFINED

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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