Clearance Summary
THE PROMA PERCEPTION, RESPONSE AND COMPASS SYSTEM AND ACCESSORIES received FDA 510(k) clearance under submission number K980106, sponsored by Proma, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1998-08-03.
- Submission: K980106
- Applicant / Sponsor: Proma, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1998-08-03
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.