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MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR

K873580 Class II Traditional
Decision Date
1987-11-02
Sponsor / Applicant
Medical High Technology International, Inc.

Technical Specification

510(k) Submission ID K873580
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 1987-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR received FDA 510(k) clearance under submission number K873580, sponsored by Medical High Technology International, 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 1987-11-02.

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.