Clearance Summary
DIAMED MODELS 600, 900, 960, 964 received FDA 510(k) clearance under submission number K854953, sponsored by Diamed Division Ill. Tool Works, 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 1986-04-22.
- Submission: K854953
- Applicant / Sponsor: Diamed Division Ill. Tool Works, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 1986-04-22
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.