ODONCER— 510(k) K062102
Substantially EquivalentTeknimed, S.A.
FDA 510(k) clearance K062102 for ODONCER, Substantially Equivalent on 2007-04-16. Applicant: Teknimed, S.A.. Device class: 2.
Clearance details
- Applicant
- Teknimed, S.A.
- Product code
- Code LYC
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Round Rock, TX, US
Recent devices under product code LYC
view allMore clearances from Teknimed, S.A.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.