DentalMonitoring
FDA 510(k) clearance DEN230035 · decided 2024-05-17
Clearance details
- K-number
- DEN230035
- Device name
- DentalMonitoring
- Applicant
- Dental Monitoring Sas
- Decision
- Unknown
- Date received
- 2023-05-04
- Decision date
- 2024-05-17
- Days to decision
- 379 days
- Clearance type
- Direct
- Product code
- SBC
- Device class
- 2
- Regulation number
- 872.1770
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Paris, FR
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.