D-SIGN III (R&D PROJECT DW264#7)— 510(k) K990077
Substantially EquivalentIvoclar North America, Inc.
FDA 510(k) clearance K990077 for D-SIGN III (R&D PROJECT DW264#7), Substantially Equivalent on 1999-02-12. Applicant: Ivoclar North America, Inc.. Device class: 2.
Clearance details
- Applicant
- Ivoclar North America, 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
Recent devices under product code EJS
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