Clearance Summary
WIRE, GUIDE - MODIFICATION received FDA 510(k) clearance under submission number K850828, sponsored by Lake Region Mfg., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-06-26.
- Submission: K850828
- Applicant / Sponsor: Lake Region Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1330
- Decision date: 1985-06-26
Classification & Regulation
This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.