ReminGel— 510(k) K241489
Substantially EquivalentInter-Med, Inc.
FDA 510(k) clearance K241489 for ReminGel, Substantially Equivalent on 2025-01-08. Applicant: Inter-Med, Inc.. Device class: 2.
Clearance details
- Applicant
- Inter-Med, 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
- Racine, WI, US
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