Clearance Summary
DLMS-ZIRBLOCKS received FDA 510(k) clearance under submission number K082137, sponsored by Dental Milling Laboratory Supplies (Dlms). The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-02-10.
- Submission: K082137
- Applicant / Sponsor: Dental Milling Laboratory Supplies (Dlms)
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2009-02-10
Classification & Regulation
This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.