Clearance Summary
SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES received FDA 510(k) clearance under submission number K941710, sponsored by Scimed Peripheral Interventions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1994-09-01.
- Submission: K941710
- Applicant / Sponsor: Scimed Peripheral Interventions
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1330
- Decision date: 1994-09-01
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.