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REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804

K062251 Class II Traditional
Decision Date
2006-10-20
Sponsor / Applicant
St Jude Medical

Technical Specification

510(k) Submission ID K062251
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 2006-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804 received FDA 510(k) clearance under submission number K062251, sponsored by St Jude Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.