Clearance Summary
MODEL 2600 PROCART received FDA 510(k) clearance under submission number K941476, sponsored by Compressor Technologies, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-09-02.
- Submission: K941476
- Applicant / Sponsor: Compressor Technologies, Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1994-09-02
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.