Osstell Beacon— 510(k) K181888
Substantially EquivalentOsstell AB
FDA 510(k) clearance K181888 for Osstell Beacon, Substantially Equivalent on 2019-08-22. Applicant: Osstell AB. Device class: 1.
Clearance details
- Applicant
- Osstell AB
- Product code
- Code EKX
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gotenborg, SE
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