Clearance Summary
INTERCEPT T.E.N.S. DEVICE received FDA 510(k) clearance under submission number K880492, sponsored by Medical Design & Manufacturing 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 1988-04-18.
- Submission: K880492
- Applicant / Sponsor: Medical Design & Manufacturing Corp.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 1988-04-18
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.