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TELSTAR BIPLANE DIGITAL IMAGING SYSTEM [TIS] MODEL 030-000915

K022565 Class II Special
Decision Date
2002-10-08
Sponsor / Applicant
Stereotaxis, Inc.

Technical Specification

510(k) Submission ID K022565
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2002-10-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELSTAR BIPLANE DIGITAL IMAGING SYSTEM [TIS] MODEL 030-000915 received FDA 510(k) clearance under submission number K022565, sponsored by Stereotaxis, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-10-08.

Classification & Regulation

This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.