FDA 510(k), K213562, DTX Studio Clinic 3.0

510(K) Number: K213562
Device Name: DTX Studio Clinic 3.0
Manufacturer: Nobel Biocare AB
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 11/09/2021
Decision Date: 03/25/2022
Regulation Medical Specialty: Radiology

424 pages (6,132 of 6,556 pages are fully redacted)