Demi Ultra— 510(k) K163064
Substantially EquivalentKerr Corporation
FDA 510(k) clearance K163064 for Demi Ultra, Substantially Equivalent on 2017-07-18. Applicant: Kerr Corporation. Device class: 2.
Clearance details
- Applicant
- Kerr Corporation
- Product code
- Code EBZ
- Device class
- Class 2
- Regulation
- 21 CFR 872.6070
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Orange, CA, US
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