CERAPEARL— 510(k) K854763
Substantially EquivalentKyocera International, Inc.
FDA 510(k) clearance K854763 for CERAPEARL, Substantially Equivalent on 1986-02-21. Applicant: Kyocera International, Inc.. Device class: 2.
Clearance details
- Applicant
- Kyocera International, Inc.
- Product code
- Code EIH
- Device class
- Class 2
- Regulation
- 21 CFR 872.6660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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