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ISOCENTRIC BEAM CHECKER

K993959 Class II Traditional
Decision Date
2000-02-14
Sponsor / Applicant
Mick Radio-Nuclear Instruments, Inc.

Technical Specification

510(k) Submission ID K993959
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2000-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISOCENTRIC BEAM CHECKER received FDA 510(k) clearance under submission number K993959, sponsored by Mick Radio-Nuclear Instruments, 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 2000-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.