DUO1 and DUO2— 510(k) K241649
Substantially EquivalentZinnovi, Inc.
FDA 510(k) clearance K241649 for DUO1 and DUO2, Substantially Equivalent on 2024-07-05. Applicant: Zinnovi, Inc.. Device class: 2.
Clearance details
- Applicant
- Zinnovi, Inc.
- Product code
- Code MUH
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Schaumburg, IL, US
Recent devices under product code MUH
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