FILTEK SUPREME ULTRA UNIVERSAL RESTORATIVE— 510(k) K083610
Substantially Equivalent3M Company
FDA 510(k) clearance K083610 for FILTEK SUPREME ULTRA UNIVERSAL RESTORATIVE, Substantially Equivalent on 2008-12-17. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code EBF
- Device class
- Class 2
- Regulation
- 21 CFR 872.3690
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.