RDT3 HANDPIECE HEAD MODEL RDT3— 510(k) K101172
Substantially EquivalentRedent Nova, Ltd.
FDA 510(k) clearance K101172 for RDT3 HANDPIECE HEAD MODEL RDT3, Substantially Equivalent on 2010-07-27. Applicant: Redent Nova, Ltd..
Clearance details
- Applicant
- Redent Nova, Ltd.
- Product code
- Code EFA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.