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EXEL 1800 AND 1800E CT SCANNER

K884670 Class II Traditional
Decision Date
1989-01-18
Sponsor / Applicant
Elscint, Inc.

Technical Specification

510(k) Submission ID K884670
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1989-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXEL 1800 AND 1800E CT SCANNER received FDA 510(k) clearance under submission number K884670, sponsored by Elscint, 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 1989-01-18.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.