Clearance Summary
IONOBOND received FDA 510(k) clearance under submission number K905724, sponsored by Micro-Vac, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-02-19.
- Submission: K905724
- Applicant / Sponsor: Micro-Vac, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3250
- Decision date: 1991-02-19
Classification & Regulation
This clearance is catalogued under FDA product code EJK and 21 CFR 872.3250, within the Dental review panel as a Class II device.