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ACHIEVE PROGRAMMABLE AUOMATED BIOPSY SYSTEMS

K141552 Class II Traditional
Decision Date
2014-09-05
Sponsor / Applicant
Care Fusion

Technical Specification

510(k) Submission ID K141552
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2014-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACHIEVE PROGRAMMABLE AUOMATED BIOPSY SYSTEMS received FDA 510(k) clearance under submission number K141552, sponsored by Care Fusion. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2014-09-05.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.