GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS— 510(k) K102307
Substantially EquivalentGenoss Co., Ltd.
FDA 510(k) clearance K102307 for GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS, Substantially Equivalent on 2011-05-04. Applicant: Genoss Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Genoss 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
- Cypress, CA, US
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