Clearance Summary
MYLAR WINDOW-TABLE INSERT PANEL received FDA 510(k) clearance under submission number K800791, sponsored by Radiation Products Design, 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 1980-05-14.
- Submission: K800791
- Applicant / Sponsor: Radiation Products Design, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 1980-05-14
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.