MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM— 510(k) K041385

Name: FDA 510(k) clearance K041385
Creator: U.S. Food and Drug Administration
Published: 2004-06-07

Substantially Equivalent

Schick Technologies, Inc.

FDA 510(k) clearance K041385 for MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM, Substantially Equivalent on 2004-06-07. Applicant: Schick Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Schick Technologies, Inc.
Product code: Code EAP
Device class: Class 2
Regulation: 21 CFR 872.1810
Advisory panel: Dental
Date received: 2004-05-25
Decision date: 2004-06-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EAP

view all

K113360 — MEDICAL IMAGE PROCESSING UNIT2012-02-07
K102573 — PROVU (TM) DENTAL X-RAY SYSTEM2011-06-30
K093453 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM2009-11-30
K080738 — DENTRON SENSOR2008-05-13
K052422 — THE ENVISION INTRAORAL DENTAL X-RAY MACHINES (WALL MOUNTED AND MOBILE)2005-09-27

More clearances from Schick Technologies, Inc.

view all

K110768 — COMPUTED DENTAL RADIOGRAPHY2011-04-20
K072134 — SCHICK COMPUTED ORAL RADIOLOGY SYSTEM2007-11-02
K053558 — CEPH, MODEL 49002006-02-17
K031291 — CDR PANX, MODEL 47922003-05-05
K022953 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM2002-10-02

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