Clearance Summary
MEDI-STIM, MODIFICATION received FDA 510(k) clearance under submission number K933237, sponsored by Mid-Canada Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1994-09-08.
- Submission: K933237
- Applicant / Sponsor: Mid-Canada Medical
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 1994-09-08
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.