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PHILIPS MODEL SL75-10 LINEAR ACCELERATOR

K870525 Class II Traditional
Decision Date
1987-04-01
Sponsor / Applicant
Industrial Accelerator Co.

Technical Specification

510(k) Submission ID K870525
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 1987-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHILIPS MODEL SL75-10 LINEAR ACCELERATOR received FDA 510(k) clearance under submission number K870525, sponsored by Industrial Accelerator Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1987-04-01.

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.