MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM— 510(k) K022953

Name: FDA 510(k) clearance K022953
Creator: U.S. Food and Drug Administration
Published: 2002-10-02

Substantially Equivalent

Schick Technologies, Inc.

FDA 510(k) clearance K022953 for MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM, Substantially Equivalent on 2002-10-02. Applicant: Schick Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Schick Technologies, Inc.
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2002-09-05
Decision date: 2002-10-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MUH

view all

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 Schick Technologies, Inc.

view all

K110768 — COMPUTED DENTAL RADIOGRAPHY2011-04-20
K093453 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM2009-11-30
K072134 — SCHICK COMPUTED ORAL RADIOLOGY SYSTEM2007-11-02
K053558 — CEPH, MODEL 49002006-02-17
K041385 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM2004-06-07

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