Cleared Traditional

K061214 - AQUARIUSAPS SERVER (FDA 510(k) Clearance)

May 2006
Decision
13d
Days
Class 2
Risk

K061214 is an FDA 510(k) clearance for the AQUARIUSAPS SERVER. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Terarecon,Inc. (San Mateo, US). The FDA issued a Cleared decision on May 15, 2006, 13 days after receiving the submission on May 2, 2006.

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

Submission Details

510(k) Number K061214 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 02, 2006
Decision Date May 15, 2006
Days to Decision 13 days
Submission Type Traditional
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