NUPRO MODEL 13016901— 510(k) K103160
Substantially EquivalentCAO Group, Inc.
FDA 510(k) clearance K103160 for NUPRO MODEL 13016901, Substantially Equivalent on 2011-01-06. Applicant: CAO Group, Inc.. Device class: 2.
Clearance details
- Applicant
- CAO Group, Inc.
- Product code
- Code LBH
- Device class
- Class 2
- Regulation
- 21 CFR 872.3260
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Jordan, UT, US
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