GUIDOR(TM)— 510(k) K912724
Substantially Equivalent for Some IndicationsProcordia Oratech AB
FDA 510(k) clearance K912724 for GUIDOR(TM), Substantially Equivalent for Some Indications on 1993-05-13. Applicant: Procordia Oratech AB. Device class: 2.
Clearance details
- Applicant
- Procordia Oratech AB
- Product code
- Code NPK
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Huddinge, Sweden, SE
Recent devices under product code NPK
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