Clearance Summary
MODIFIED PERIPHERAL DILATATION CATHETERS received FDA 510(k) clearance under submission number K875175, sponsored by Schneider-Shilley (Usa). The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-07-28.
- Submission: K875175
- Applicant / Sponsor: Schneider-Shilley (Usa)
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1988-07-28
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.