Clearance Summary
MULTISAFE POWDER FREE NITRILE GLOVES, NON STERILE (BLUE) received FDA 510(k) clearance under submission number K001619, sponsored by Multisafe Sdn. Bhd.. 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 2000-07-26.
- Submission: K001619
- Applicant / Sponsor: Multisafe Sdn. Bhd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2000-07-26
Classification & Regulation
This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.