KJ MASK— 510(k) K103019
Substantially EquivalentKj Meditech Co., Ltd.
FDA 510(k) clearance K103019 for KJ MASK, Substantially Equivalent on 2011-06-09. Applicant: Kj Meditech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Kj Meditech Co., Ltd.
- Product code
- Code DZB
- Device class
- Class 2
- Regulation
- 21 CFR 872.5500
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fullerton, CA, US
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