meddevicedb.com FDA Device Reference

UPACS

K960941 Class I Traditional
Decision Date
1996-06-03
Sponsor / Applicant
Base Ten Systems, Inc.

Technical Specification

510(k) Submission ID K960941
Product Code LMB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2010
Decision Date 1996-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UPACS received FDA 510(k) clearance under submission number K960941, sponsored by Base Ten Systems, 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 1996-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code LMB and 21 CFR 892.2010, within the Radiology review panel as a Class I device.