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RX ACCUNET LP EMBOLIC PROTECTION SYSTEM

K081549 Class II Traditional
Decision Date
2008-08-19
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K081549
Product Code NTE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2008-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RX ACCUNET LP EMBOLIC PROTECTION SYSTEM received FDA 510(k) clearance under submission number K081549, sponsored by Abbott Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-08-19.

Classification & Regulation

This clearance is catalogued under FDA product code NTE and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.