ContaCT— 510(k) DEN170073
UnknownViz.Al, Inc.
FDA 510(k) clearance DEN170073 for ContaCT, Unknown on 2018-02-13. Applicant: Viz.Al, Inc.. Device class: 2.
Clearance details
- Applicant
- Viz.Al, Inc.
- Product code
- Code QAS
- Device class
- Class 2
- Regulation
- 21 CFR 892.2080
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Francisco, CA, US
Recent devices under product code QAS
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