Clearance Summary
MODIFICATION TO IMTEC SENDAX MDI received FDA 510(k) clearance under submission number K990983, sponsored by Imtec Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1999-04-13.
- Submission: K990983
- Applicant / Sponsor: Imtec Corp.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 1999-04-13
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.