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RTI MEDICAL

K954567 Class I Traditional
Decision Date
1996-04-12
Sponsor / Applicant
Radiology Telenetwork Intl.

Technical Specification

510(k) Submission ID K954567
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1996-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RTI MEDICAL received FDA 510(k) clearance under submission number K954567, sponsored by Radiology Telenetwork Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code LMD and 21 CFR 892.2020, within the Radiology review panel as a Class I device.