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APAX PACS SYSTEM

K032760 Class II Traditional
Decision Date
2003-09-17
Sponsor / Applicant
Tis, Inc.

Technical Specification

510(k) Submission ID K032760
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2003-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APAX PACS SYSTEM received FDA 510(k) clearance under submission number K032760, sponsored by Tis, 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 2003-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.