ZIRTOUGH— 510(k) K133211
Substantially EquivalentKuraray Noritake Dental, Inc.
FDA 510(k) clearance K133211 for ZIRTOUGH, Substantially Equivalent on 2014-03-20. Applicant: Kuraray Noritake Dental, Inc.. Device class: 2.
Clearance details
- Applicant
- Kuraray Noritake Dental, Inc.
- Product code
- Code EIH
- Device class
- Class 2
- Regulation
- 21 CFR 872.6660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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