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PREPSTAIN (TM) SYSTEM

FDA premarket approval P970018/S006 · decided 2003-05-02

Approval details

PMA number
P970018
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
PREPSTAIN (TM) SYSTEM
Generic name
Processor, cervical cytology slide, automated
Applicant
Bd Diagnostic Systems
Date received
2003-03-24
Decision date
2003-05-02
Days to decision
39 days
Decision code
APPR
Product code
MKQ
Advisory committee
Pathology
Expedited review
No
Location
Durham, NC
Statement
APPROVAL TO MODIFY THE CURRENT APPROVED LABELING TO INCLUDE DATA AND INFORMATION FROM A DIRECT-TO-VIAL CLINICAL STUDY FOR HIGH GRADE SQUAMOUS INTRAEPITHELIAL AND MORE SEVERE LESIONS.

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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