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PROSIGNA BREAST CANCER PROGNOSTIC GENE SIGNATURE ASSAY

K141771 Class II Traditional
Decision Date
2014-11-07
Sponsor / Applicant
Nanostring Technologies, Inc.

Technical Specification

510(k) Submission ID K141771
Product Code NYI
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6040
Decision Date 2014-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROSIGNA BREAST CANCER PROGNOSTIC GENE SIGNATURE ASSAY received FDA 510(k) clearance under submission number K141771, sponsored by Nanostring Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2014-11-07.

Classification & Regulation

This clearance is catalogued under FDA product code NYI and 21 CFR 866.6040, within the Immunology review panel as a Class II device.