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MODEL-BASED RSA SOFTWARE

K133966 Class II Traditional
Decision Date
2014-03-06
Sponsor / Applicant
Halifax Biomedical, Inc.

Technical Specification

510(k) Submission ID K133966
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2014-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL-BASED RSA SOFTWARE received FDA 510(k) clearance under submission number K133966, sponsored by Halifax Biomedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.