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DIGITAL DISK RECORDER(DDR) W/NUMERICAL SUFFIXES

K905111 Class II Traditional
Decision Date
1991-01-25
Sponsor / Applicant
Eigen

Technical Specification

510(k) Submission ID K905111
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1991-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGITAL DISK RECORDER(DDR) W/NUMERICAL SUFFIXES received FDA 510(k) clearance under submission number K905111, sponsored by Eigen. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.