Clearance Summary
SUN-LITE WHITE SPOT received FDA 510(k) clearance under submission number K841588, sponsored by Suncoast Medical Manufacturers, Inc.. 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 1984-05-22.
- Submission: K841588
- Applicant / Sponsor: Suncoast Medical Manufacturers, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6350
- Decision date: 1984-05-22
Classification & Regulation
This clearance is catalogued under FDA product code KYT and 21 CFR 880.6350, within the General Hospital review panel as a Class I device.