Cleared Special

K222072 - Dolphin Imaging 12.0 (FDA 510(k) Clearance)

Aug 2022
Decision
25d
Days
Class 2
Risk

K222072 is an FDA 510(k) clearance for the Dolphin Imaging 12.0. 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 August 8, 2022, 25 days after receiving the submission on July 14, 2022.

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

Submission Details

510(k) Number K222072 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 14, 2022
Decision Date August 08, 2022
Days to Decision 25 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