Clearance Summary
LATEX FINGER COTS received FDA 510(k) clearance under submission number K903073, sponsored by Dongkuk Trading Co., Ltd.. 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 1990-09-12.
- Submission: K903073
- Applicant / Sponsor: Dongkuk Trading Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1990-09-12
Classification & Regulation
This clearance is catalogued under FDA product code LZB and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.