FDA PMA FDA Class 3 Approved 🇺🇸 United States

Processor, Cervical Cytology Slide, Automated

PMA: P970018 · Supplement: S031 · Decision Jun 14, 2015
Classifications
1
FEI Numbers
7
Registration Numbers
7

Basic Information

Device Name
Processor, Cervical Cytology Slide, Automated
Trade Name
BD PREPMATE SLIDE PROCESSOR, BD PREPMATE AUTOMATED ACCESSORY
PMA Number
P970018
Supplement Number
S031
Device Class
FDA Class 3
Product Code
MKQ
Generic Name
Processor, cervical cytology slide, automated
Medical Specialty
Unknown
Advisory Committee
Pathology
Decision
Approved
Decision Code
APPR
Decision Date
June 14, 2015
Date Received
January 22, 2015
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MANUFACTURING SITE LOCATED SPARKS, MD.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MKQ Processor, Cervical Cytology Slide, Automated