FDA 510(k) Applications Submitted by SCHICK TECHNOLOGIES, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K001429 |
05/05/2000 |
MODIFICATION TO ACCUDEXA BONE DENSITOMETER |
SCHICK TECHNOLOGIES, INC. |
K041385 |
05/25/2004 |
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM |
SCHICK TECHNOLOGIES, INC. |
K022953 |
09/05/2002 |
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM |
SCHICK TECHNOLOGIES, INC. |
K053558 |
12/21/2005 |
CEPH, MODEL 4900 |
SCHICK TECHNOLOGIES, INC. |
K072134 |
08/02/2007 |
SCHICK COMPUTED ORAL RADIOLOGY SYSTEM |
SCHICK TECHNOLOGIES, INC. |
K031291 |
04/23/2003 |
CDR PANX, MODEL 4792 |
SCHICK TECHNOLOGIES, INC. |
K982661 |
07/30/1998 |
CDR - PAN MODEL 4700 |
SCHICK TECHNOLOGIES, INC. |
K963778 |
09/20/1996 |
CDR-CAM |
SCHICK TECHNOLOGIES, INC. |
K093453 |
11/05/2009 |
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM |
SCHICK TECHNOLOGIES, INC. |
K110768 |
03/18/2011 |
COMPUTED DENTAL RADIOGRAPHY |
SCHICK TECHNOLOGIES, INC. |
K981124 |
03/27/1998 |
ACCUDEXA BONE DENSITOMETER |
SCHICK TECHNOLOGIES, INC. |
K971735 |
05/12/1997 |
ACCUDEXA BONE DENSITOMETER |
SCHICK TECHNOLOGIES, INC. |
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