OssGuide— 510(k) K200623
Substantially EquivalentSk Bioland Co., Ltd.
FDA 510(k) clearance K200623 for OssGuide, Substantially Equivalent on 2020-10-02. Applicant: Sk Bioland Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Sk Bioland Co., Ltd.
- Product code
- Code NPL
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cheongju-Si, KR
Recent devices under product code NPL
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