Clearance Summary
DREAM DAM received FDA 510(k) clearance under submission number K875255, sponsored by Dental Dam, 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 1988-03-18.
- Submission: K875255
- Applicant / Sponsor: Dental Dam, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6300
- Decision date: 1988-03-18
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.