BioMin Restore Plus— 510(k) K200077
Substantially EquivalentDr. Collins, Inc.
FDA 510(k) clearance K200077 for BioMin Restore Plus, Substantially Equivalent on 2020-11-06. Applicant: Dr. Collins, Inc.. Device class: 2.
Clearance details
- Applicant
- Dr. Collins, Inc.
- Product code
- Code LBH
- Device class
- Class 2
- Regulation
- 21 CFR 872.3260
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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