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SIS 2000 MAMMOGRAPHIC X-RAY SYSTEM

K885127 Class II Traditional
Decision Date
1989-02-16
Sponsor / Applicant
Fischer Imaging Corp.

Technical Specification

510(k) Submission ID K885127
Product Code LMC
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2040
Decision Date 1989-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS 2000 MAMMOGRAPHIC X-RAY SYSTEM received FDA 510(k) clearance under submission number K885127, sponsored by Fischer Imaging 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 1989-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code LMC and 21 CFR 892.2040, within the Radiology review panel as a Class II device.