Clearance Summary
BioHPP - breCAM.BioHPP received FDA 510(k) clearance under submission number K152113, sponsored by Bredent GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-07-21.
- Submission: K152113
- Applicant / Sponsor: Bredent GmbH & Co. KG
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2016-07-21
Classification & Regulation
This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.