Clearance Summary
NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER received FDA 510(k) clearance under submission number K952884, sponsored by Meadox Medicals, Div. Boston Scientific Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-02-21.
- Submission: K952884
- Applicant / Sponsor: Meadox Medicals, Div. Boston Scientific Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1996-02-21
Classification & Regulation
This clearance is catalogued under FDA product code LIT and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.