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THROMCAT THROMBECTOMY CATHETER SYSTEM

K060016 Class II Traditional
Decision Date
2006-04-25
Sponsor / Applicant
Kensey Nash Corp.

Technical Specification

510(k) Submission ID K060016
Product Code MCW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4875
Decision Date 2006-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THROMCAT THROMBECTOMY CATHETER SYSTEM received FDA 510(k) clearance under submission number K060016, sponsored by Kensey Nash 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 2006-04-25.

Classification & Regulation

This clearance is catalogued under FDA product code MCW and 21 CFR 870.4875, within the Cardiovascular review panel as a Class II device.