Cleared Traditional

K200755 - Caption Guidance (FDA 510(k) Clearance)

Apr 2020
Decision
24d
Days
Class 2
Risk

K200755 is an FDA 510(k) clearance for the Caption Guidance. This device is classified as a Image Acquisition And/or Optimization Guided By Artificial Intelligence (Class II - Special Controls, product code QJU).

Submitted by Caption Health (Brisbane, US). The FDA issued a Cleared decision on April 16, 2020, 24 days after receiving the submission on March 23, 2020.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2100. A Radiological Acquisition And/or Optimization Guidance System Is A Device That Is Intended To Aid In The Acquisition And/or Optimization Of Images And/or Diagnostic Signals. The Device Interfaces With The Acquisition System, Analyzes Its Output, And Provides Guidance And/or Feedback To The Operator For Improving Image And/or Signal Quality..

Submission Details

510(k) Number K200755 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 2020
Decision Date April 16, 2020
Days to Decision 24 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code QJU - Image Acquisition And/or Optimization Guided By Artificial Intelligence
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2100
Definition A Radiological Acquisition And/or Optimization Guidance System Is A Device That Is Intended To Aid In The Acquisition And/or Optimization Of Images And/or Diagnostic Signals. The Device Interfaces With The Acquisition System, Analyzes Its Output, And Provides Guidance And/or Feedback To The Operator For Improving Image And/or Signal Quality.