Clearance Summary
RAYMAX 2100 MODELS 2130 & 2136 received FDA 510(k) clearance under submission number K883431, sponsored by Raymax Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1988-09-12.
- Submission: K883431
- Applicant / Sponsor: Raymax Medical Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1700
- Decision date: 1988-09-12
Classification & Regulation
This clearance is catalogued under FDA product code IZO and 21 CFR 892.1700, within the Radiology review panel as a Class I device.