DISCOID/CLEOID DOUBLE END AMALGAM CARVER— 510(k) K901177
Substantially EquivalentAmerican Medical Ceramics, Inc.
FDA 510(k) clearance K901177 for DISCOID/CLEOID DOUBLE END AMALGAM CARVER, Substantially Equivalent on 1990-04-16. Applicant: American Medical Ceramics, Inc.. Device class: 1.
Clearance details
- Applicant
- American Medical Ceramics, Inc.
- Product code
- Code EKJ
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Knoxville, TN, US
Recent devices under product code EKJ
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