D.SIGN 59— 510(k) K013809
Substantially EquivalentIvoclar Vivadent, Inc.
FDA 510(k) clearance K013809 for D.SIGN 59, Substantially Equivalent on 2002-02-07. Applicant: Ivoclar Vivadent, Inc.. Device class: 2.
Clearance details
- Applicant
- Ivoclar Vivadent, Inc.
- Product code
- Code EJS
- Device class
- Class 2
- Regulation
- 21 CFR 872.3060
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
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