Tristel Duo ULT— 510(k) DEN220041
UnknownTristel Solutions Limited
FDA 510(k) clearance DEN220041 for Tristel Duo ULT, Unknown on 2023-06-02. Applicant: Tristel Solutions Limited. Device class: 2.
Clearance details
- Applicant
- Tristel Solutions Limited
- Product code
- Code QWS
- Device class
- Class 2
- Regulation
- 21 CFR 880.6886
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Snailwell, GB
Recent devices under product code QWS
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