FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Processor, Cervical Cytology Slide, Automated

PMA: P040052 · Supplement: S007 · Decision Oct 1, 2008
Classifications
1
FEI Numbers
7
Registration Numbers
7

Basic Information

Device Name
Processor, Cervical Cytology Slide, Automated
Trade Name
MONOPREP PAP TEST
PMA Number
P040052
Supplement Number
S007
Device Class
FDA Class 3
Product Code
MKQ
Generic Name
Processor, cervical cytology slide, automated
Medical Specialty
Unknown
Advisory Committee
Pathology
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
October 1, 2008
Date Received
September 2, 2008
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

CHANGE OF VENDOR TO PHARMCO-AAPER FOR THE ALCOHOL-BASED SPECIMEN TRANSPORT SOLUTION (MPPT-STS) THAT PRESERVES SPECIMEN CELLULAR MORPHOLOGY AND INHIBITS MICROBIAL GROWTH.

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