Clearance Summary
EP 3000 received FDA 510(k) clearance under submission number K924879, sponsored by Oec-Diasonics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1993-01-04.
- Submission: K924879
- Applicant / Sponsor: Oec-Diasonics, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 1993-01-04
Classification & Regulation
This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.