Clearance Summary
LATEX EXAM GLOVES (MFG. KOSSAN LATEX INDUSTRIES) received FDA 510(k) clearance under submission number K892319, sponsored by Svenska Medita Ac.. 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 1989-08-22.
- Submission: K892319
- Applicant / Sponsor: Svenska Medita Ac.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1989-08-22
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.