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ELITE R/F SPOT FILM DRIVE

K902403 Class II Traditional
Decision Date
1990-08-01
Sponsor / Applicant
Rms Div.

Technical Specification

510(k) Submission ID K902403
Product Code IXL
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1670
Decision Date 1990-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELITE R/F SPOT FILM DRIVE received FDA 510(k) clearance under submission number K902403, sponsored by Rms Div.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-08-01.

Classification & Regulation

This clearance is catalogued under FDA product code IXL and 21 CFR 892.1670, within the Radiology review panel as a Class II device.