Clearance Summary
RADIONICS POLE NEEDLES received FDA 510(k) clearance under submission number K021942, sponsored by Radionics, A Division of Tyco Healthcare Group LP. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2002-09-11.
- Submission: K021942
- Applicant / Sponsor: Radionics, A Division of Tyco Healthcare Group LP
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4725
- Decision date: 2002-09-11
Classification & Regulation
This clearance is catalogued under FDA product code GXI and 21 CFR 882.4725, within the Neurology review panel as a Class II device.