FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Reader, Cervical Cytology Slide, Automated
PMA: P020002
·
Supplement: S003
·
Decision Aug 30, 2007
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- Reader, Cervical Cytology Slide, Automated
- Trade Name
- THINPREP IMAGING SYSTEM
- PMA Number
- P020002
- Supplement Number
- S003
- Device Class
- FDA Class 3
- Product Code
- MNM
- Generic Name
- READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED
- Medical Specialty
- Unknown
- Advisory Committee
- Pathology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- August 30, 2007
- Date Received
- July 11, 2007
- 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 AT CYTYC, MARLBOROUGH, MASSACHUSETTS.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MNM | Reader, Cervical Cytology Slide, Automated | FDA class 3 | Unknown |