Clearance Summary
GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE received FDA 510(k) clearance under submission number K993793, sponsored by Guthrie Medicare Products (Melaka) 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 2000-01-12.
- Submission: K993793
- Applicant / Sponsor: Guthrie Medicare Products (Melaka) Sdn Bhd
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2000-01-12
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.