Radify Triage— 510(k) K231871
Substantially EquivalentEnvisionit Deepai, Ltd.
FDA 510(k) clearance K231871 for Radify Triage, Substantially Equivalent on 2024-01-17. Applicant: Envisionit Deepai, Ltd.. Device class: 2.
Clearance details
- Applicant
- Envisionit Deepai, Ltd.
- Product code
- Code QFM
- Device class
- Class 2
- Regulation
- 21 CFR 892.2080
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Cobham, GB
Recent devices under product code QFM
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