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DIGITAL ADD ON MULTI SYSTEM

K973710 Class II Traditional
Decision Date
1997-12-18
Sponsor / Applicant
Swissray International, Inc.

Technical Specification

510(k) Submission ID K973710
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 1997-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGITAL ADD ON MULTI SYSTEM received FDA 510(k) clearance under submission number K973710, sponsored by Swissray International, 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 1997-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.