ECUSIT COMPOSITE REPAIR— 510(k) K992879
Substantially EquivalentDmg Hamburg
FDA 510(k) clearance K992879 for ECUSIT COMPOSITE REPAIR, Substantially Equivalent on 1999-11-09. Applicant: Dmg Hamburg. Device class: 2.
Clearance details
- Applicant
- Dmg Hamburg
- Product code
- Code KLE
- Device class
- Class 2
- Regulation
- 21 CFR 872.3200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ayer, MA, US
Recent devices under product code KLE
view allData sourced from openFDA. This site is unofficial and independent of the FDA.