CLEARFIL DC ACTIVATOR; CLEARFIL DC ACTIVATOR TRIAL— 510(k) K131430
Substantially EquivalentKuraray Noritake Dental, Inc.
FDA 510(k) clearance K131430 for CLEARFIL DC ACTIVATOR; CLEARFIL DC ACTIVATOR TRIAL, Substantially Equivalent on 2013-08-30. Applicant: Kuraray Noritake Dental, Inc..
Clearance details
- Applicant
- Kuraray Noritake Dental, Inc.
- Product code
- Code KLE
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chiyoda-Ku, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.