Clearance Summary
DENSPRO MEDIUM MINT PROPHY PASTE received FDA 510(k) clearance under submission number K923675, sponsored by Teledyne Getz. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-11-05.
- Submission: K923675
- Applicant / Sponsor: Teledyne Getz
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6030
- Decision date: 1992-11-05
Classification & Regulation
This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.