VarioSurg 4— 510(k) K254163
Substantially EquivalentNakanishi, Inc.
FDA 510(k) clearance K254163 for VarioSurg 4, Substantially Equivalent on 2025-12-23. Applicant: Nakanishi, Inc.. Device class: 2.
Clearance details
- Applicant
- Nakanishi, Inc.
- Product code
- Code DZI
- Device class
- Class 2
- Regulation
- 21 CFR 872.4120
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kanuma, JP
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