Cleared Traditional

Second Opinion? BLE

K243230 · Pearl, Inc. · Radiology
May 2025
Decision
213d
Days
Class 2
Risk

About This 510(k) Submission

K243230 is an FDA 510(k) clearance for the Second Opinion? BLE, a Automated Radiological Image Processing Software (Class II — Special Controls, product code QIH), submitted by Pearl, Inc. (Beverly Hills, US). The FDA issued a Cleared decision on May 9, 2025, 213 days after receiving the submission on October 8, 2024. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K243230 FDA.gov
FDA Decision Cleared SESE
Date Received October 08, 2024
Decision Date May 09, 2025
Days to Decision 213 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code QIH — Automated Radiological Image Processing Software
Device Class Class II — Special Controls
CFR Regulation 21 CFR 892.2050
Definition To Provide Automated Radiological Image Processing And Analysis Tools. Software Implementing Artificial Intelligence Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Data. In These Devices, The Algorithm Training Data Typically Impacts Device Performance. Adaptive Ai Algorithms Are Not Within Scope Of This Product Code.