Cleared Traditional

K221478 - Dolphin Blue Imaging (FDA 510(k) Clearance)

Nov 2022
Decision
162d
Days
Class 2
Risk

K221478 is an FDA 510(k) clearance for the Dolphin Blue Imaging. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Patterson Dental Supply, Inc. (Chatsworth, US). The FDA issued a Cleared decision on November 1, 2022, 162 days after receiving the submission on May 23, 2022.

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

Submission Details

510(k) Number K221478 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 2022
Decision Date November 01, 2022
Days to Decision 162 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