ACORN ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE— 510(k) K960565
Substantially EquivalentDent Zar, Inc.
FDA 510(k) clearance K960565 for ACORN ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE, Substantially Equivalent on 1996-03-22. Applicant: Dent Zar, Inc.. Device class: 2.
Clearance details
- Applicant
- Dent Zar, Inc.
- 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
- Los Angeles, CA, US
Recent devices under product code EBF
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Data sourced from openFDA. This site is unofficial and independent of the FDA.