RiX70 DC— 510(k) K182206
Substantially EquivalentTrident S.R.L
FDA 510(k) clearance K182206 for RiX70 DC, Substantially Equivalent on 2018-09-13. Applicant: Trident S.R.L. Device class: 2.
Clearance details
- Applicant
- Trident S.R.L
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Castenedolo, IT
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