KidneyIntelX.dkd— 510(k) DEN200052
UnknownRenalytix Ai, Inc.
FDA 510(k) clearance DEN200052 for KidneyIntelX.dkd, Unknown on 2023-06-29. Applicant: Renalytix Ai, Inc.. Device class: 2.
Clearance details
- Applicant
- Renalytix Ai, Inc.
- Product code
- Code QWZ
- Device class
- Class 2
- Regulation
- 21 CFR 862.1223
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.