FDA PMA FDA Class 3 Approved 🇺🇸 United States

Processor, Cervical Cytology Slide, Automated

PMA: P950039 · Supplement: S035 · Decision Oct 26, 2016
Classifications
1
FEI Numbers
7
Registration Numbers
7

Basic Information

Device Name
Processor, Cervical Cytology Slide, Automated
Trade Name
THINPREP PROCESSOR,
PMA Number
P950039
Supplement Number
S035
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
October 26, 2016
Date Received
October 5, 2016
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval of labeling changes for the ThinPrep® 3000 Processor.

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