Clearance Summary
DUFFY BOLUS INJECTOR received FDA 510(k) clearance under submission number K863936, sponsored by Viox 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 1987-01-06.
- Submission: K863936
- Applicant / Sponsor: Viox Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.6500
- Decision date: 1987-01-06
Classification & Regulation
This clearance is catalogued under FDA product code IWR and 21 CFR 892.6500, within the Radiology review panel as a Class I device.