IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013— 510(k) K960480
Substantially EquivalentVident
FDA 510(k) clearance K960480 for IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013, Substantially Equivalent on 1996-03-15. Applicant: Vident. Device class: 2.
Clearance details
- Applicant
- Vident
- Product code
- Code ELL
- Device class
- Class 2
- Regulation
- 21 CFR 872.3920
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Brea, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.