Clearance Summary
FUNNEL GUIDE CATHETER MODEL G1020608 received FDA 510(k) clearance under submission number K102439, sponsored by Lazarus Effect, 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 2012-01-12.
- Submission: K102439
- Applicant / Sponsor: Lazarus Effect, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2012-01-12
Classification & Regulation
This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.