Clearance Summary
PLANMECA INTRACAM received FDA 510(k) clearance under submission number K972033, sponsored by Planmeca Oy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1997-06-20.
- Submission: K972033
- Applicant / Sponsor: Planmeca Oy
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1997-06-20
Classification & Regulation
This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.