meddevicedb.com FDA Device Reference

RECTILINEAR SCANNER MODEL #187-270

K895799 Class I Traditional
Decision Date
1990-02-01
Sponsor / Applicant
Atomic Products Corp.

Technical Specification

510(k) Submission ID K895799
Product Code IYW
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1300
Decision Date 1990-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECTILINEAR SCANNER MODEL #187-270 received FDA 510(k) clearance under submission number K895799, sponsored by Atomic Products Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-02-01.

Classification & Regulation

This clearance is catalogued under FDA product code IYW and 21 CFR 892.1300, within the Radiology review panel as a Class I device.