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ERBIUM X-RAY FILTER

K860760 Class I Traditional
Decision Date
1986-06-10
Sponsor / Applicant
Reactor Experiments, Inc.

Technical Specification

510(k) Submission ID K860760
Product Code ITY
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1760
Decision Date 1986-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ERBIUM X-RAY FILTER received FDA 510(k) clearance under submission number K860760, sponsored by Reactor Experiments, 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 1986-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code ITY and 21 CFR 892.1760, within the Radiology review panel as a Class I device.