Clearance Summary
MINIDAM II received FDA 510(k) clearance under submission number K921771, sponsored by Delsan Dental Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-09-17.
- Submission: K921771
- Applicant / Sponsor: Delsan Dental Systems
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6300
- Decision date: 1992-09-17
Classification & Regulation
This clearance is catalogued under FDA product code EIE and 21 CFR 872.6300, within the Dental review panel as a Class I device.