RELINE-IT MODEL RELINE-IT— 510(k) K101771
Substantially EquivalentMajestic Drug Co., Inc.
FDA 510(k) clearance K101771 for RELINE-IT MODEL RELINE-IT, Substantially Equivalent on 2010-09-20. Applicant: Majestic Drug Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Majestic Drug Co., Inc.
- Product code
- Code EBP
- Device class
- Class 2
- Regulation
- 21 CFR 872.3560
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Orange, CT, US
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