Cleared Special

K072986 - INTEGRADWEB PACS SYSTEM (FDA 510(k) Clearance)

Nov 2007
Decision
28d
Days
Class 2
Risk

K072986 is an FDA 510(k) clearance for the INTEGRADWEB PACS SYSTEM. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Ge Healthcare (Monroe, US). The FDA issued a Cleared decision on November 20, 2007, 28 days after receiving the submission on October 23, 2007.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K072986 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 2007
Decision Date November 20, 2007
Days to Decision 28 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code LLZ — System, Image Processing, Radiological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050