Clearance Summary
PODIOSCOPE BY ARROW received FDA 510(k) clearance under submission number K820119, sponsored by Arrow X-Ray 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 1982-02-18.
- Submission: K820119
- Applicant / Sponsor: Arrow X-Ray Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1610
- Decision date: 1982-02-18
Classification & Regulation
This clearance is catalogued under FDA product code KPW and 21 CFR 892.1610, within the Radiology review panel as a Class II device.