S1— 510(k) K231672
Substantially EquivalentMedpark Co., Ltd.
FDA 510(k) clearance K231672 for S1, Substantially Equivalent on 2023-10-13. Applicant: Medpark Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Medpark Co., Ltd.
- Product code
- Code NPM
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buk-Gu, KR
Recent devices under product code NPM
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