K241489
- 510(k) number
- K241489
- Device name
- ReminGel
- Applicant
- Inter-Med, Inc. WI · US
- Product code
- LBH — Varnish, Cavity
- Decision date
- 2025-01-08
- Date received
- 2024-05-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K241489.pdf
Official FDA record: K241489
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.