Clearance Summary
AXON II BRAND OF DUAL CHANNEL TENS received FDA 510(k) clearance under submission number K850860, sponsored by Cassandra Electronics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1985-05-31.
- Submission: K850860
- Applicant / Sponsor: Cassandra Electronics Corp.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 1985-05-31
Classification & Regulation
This clearance is catalogued under FDA product code GZJ and 21 CFR 882.5890, within the Neurology review panel as a Class II device.