Clearance Summary
NemoCast received FDA 510(k) clearance under submission number K193003, sponsored by Software Nemotec S.L.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-06-05.
- Submission: K193003
- Applicant / Sponsor: Software Nemotec S.L.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5470
- Decision date: 2020-06-05
Classification & Regulation
This clearance is catalogued under FDA product code PNN and 21 CFR 872.5470, within the Dental review panel as a Class II device.