CLEARFIL DC CEMENT— 510(k) K980232
Substantially EquivalentKuraray Company, Ltd.
FDA 510(k) clearance K980232 for CLEARFIL DC CEMENT, Substantially Equivalent on 1998-02-24. Applicant: Kuraray Company, Ltd.. Device class: 2.
Clearance details
- Applicant
- Kuraray Company, Ltd.
- 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
- New York, NY, US
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