Clearance Summary
BURNET LABORATOIRE PHARMACEUTIQUE SURGICAL GLOVES received FDA 510(k) clearance under submission number K882392, sponsored by Roseburg SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-08-26.
- Submission: K882392
- Applicant / Sponsor: Roseburg SA
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4460
- Decision date: 1988-08-26
Classification & Regulation
This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.