TUBULITEC LINER— 510(k) K851053
Substantially EquivalentDental Therapeutics AB
FDA 510(k) clearance K851053 for TUBULITEC LINER, Substantially Equivalent on 1985-07-25. Applicant: Dental Therapeutics AB. Device class: 2.
Clearance details
- Applicant
- Dental Therapeutics AB
- Product code
- Code EJK
- Device class
- Class 2
- Regulation
- 21 CFR 872.3250
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nacka, SE
Recent devices under product code EJK
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