KODAK 9000, KODAK 9000 3D— 510(k) K073435

Substantially Equivalent

Trophy

FDA 510(k) clearance K073435 for KODAK 9000, KODAK 9000 3D, Substantially Equivalent on 2008-02-11. Applicant: Trophy. Device class: 2.

Clearance details

Applicant: Trophy
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2007-12-06
Decision date: 2008-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marne La Vallee Cedex 2, FR

Download summary PDF View on FDA.gov ↗

Recent devices under product code MUH

K251793 — SOTA Cloud Smart Sensor (1.5)2026-03-03
K252570 — EzSensor HD, EzSensor UHD2025-11-10
K250687 — Cocoon Solo (DX-7020s)2025-10-24
K251206 — Digital X-Ray DentiMax Pro Imaging System2025-09-24
K240040 — VistaPano S Ceph 2.0 (VistaPano S Ceph) +3 more2024-10-25

More clearances from Trophy

K193390 — CS Model+2020-04-02
K200183 — CS 96002020-03-13
K181136 — CS 96002018-05-24
K173622 — CS Imaging2018-01-16
K151087 — CS 8100SC, CS8100SC Access2015-08-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.