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EMI SIMULATOR REMOTE CONTROL CONSOLE

K781519 Class II Traditional
Decision Date
1978-09-14
Sponsor / Applicant
Emi Medical, Inc.

Technical Specification

510(k) Submission ID K781519
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 1978-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMI SIMULATOR REMOTE CONTROL CONSOLE received FDA 510(k) clearance under submission number K781519, sponsored by Emi Medical, 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 1978-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code KPQ and 21 CFR 892.5840, within the Radiology review panel as a Class II device.