Clearance Summary
DRI-CLAVE LIQUID KLEENZALL received FDA 510(k) clearance under submission number K880754, sponsored by Columbus Dental Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-05-12.
- Submission: K880754
- Applicant / Sponsor: Columbus Dental Mfg. Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1988-05-12
Classification & Regulation
This clearance is catalogued under FDA product code EHZ and 21 CFR 872.6640, within the Dental review panel as a Class I device.