meddevicedb.com FDA Device Reference

COMPUTE RX-PLAN

K850977 Class II Traditional
Decision Date
1985-07-26
Sponsor / Applicant
Medicalibration

Technical Specification

510(k) Submission ID K850977
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 1985-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPUTE RX-PLAN received FDA 510(k) clearance under submission number K850977, sponsored by Medicalibration. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1985-07-26.

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.