FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Somatic Gene Mutation Detection System
PMA: P110020
·
Supplement: S031
·
Decision Dec 13, 2018
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Somatic Gene Mutation Detection System
- Trade Name
- cobas BRAF V600 Mutation Test
- PMA Number
- P110020
- Supplement Number
- S031
- Device Class
- FDA Class 3
- Product Code
- OWD
- Generic Name
- Somatic gene mutation detection system
- Medical Specialty
- Unknown
- Advisory Committee
- Pathology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- December 13, 2018
- Date Received
- November 13, 2018
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Implementation of a cleaning process for pumps used in component manufacturing.
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 |
|---|---|---|---|
| OWD | Somatic Gene Mutation Detection System | FDA class 3 | Unknown |