Clearance Summary
DR. MICHAEL'S FOOT HELPER received FDA 510(k) clearance under submission number K802837, sponsored by Dr. Michael'S Foot-Care Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1980-12-10.
- Submission: K802837
- Applicant / Sponsor: Dr. Michael'S Foot-Care Products
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1980-12-10
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.