Clearance Summary
EYE SPOT RF TEST received FDA 510(k) clearance under submission number K932437, sponsored by J & S Medical Assoc., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1993-08-23.
- Submission: K932437
- Applicant / Sponsor: J & S Medical Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5775
- Decision date: 1993-08-23
Classification & Regulation
This clearance is catalogued under FDA product code DHR and 21 CFR 866.5775, within the Immunology review panel as a Class II device.