Clearance Summary
VAXIOM FAMILY OF RF LESION PROBES & ELEC received FDA 510(k) clearance under submission number K802243, sponsored by Progress Mankind Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1980-11-12.
- Submission: K802243
- Applicant / Sponsor: Progress Mankind Technology
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4725
- Decision date: 1980-11-12
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.