SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)— 510(k) K003407
Substantially EquivalentIvoclar North America, Inc.
FDA 510(k) clearance K003407 for SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER), Substantially Equivalent on 2001-01-26. Applicant: Ivoclar North America, Inc.. Device class: 2.
Clearance details
- Applicant
- Ivoclar North America, Inc.
- Product code
- Code EMA
- Device class
- Class 2
- Regulation
- 21 CFR 872.3275
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
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