A-Oss— 510(k) K151542
Substantially EquivalentHiossen, Inc.
FDA 510(k) clearance K151542 for A-Oss, Substantially Equivalent on 2016-08-03. Applicant: Hiossen, Inc.. Device class: 2.
Clearance details
- Applicant
- Hiossen, Inc.
- 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
- Fariless Hills, PA, US
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