Clearance Summary
MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM received FDA 510(k) clearance under submission number K003090, sponsored by Midmark Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-10-18.
- Submission: K003090
- Applicant / Sponsor: Midmark Corp.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 2000-10-18
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.