Clearance Summary
A-DEC 7284 CUSPIDOR, CASCADE received FDA 510(k) clearance under submission number K925367, sponsored by A-Dec, 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 1994-04-11.
- Submission: K925367
- Applicant / Sponsor: A-Dec, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1994-04-11
Classification & Regulation
This clearance is catalogued under FDA product code EBR and 21 CFR 872.6640, within the Dental review panel as a Class I device.