FDA 510(k) Applications Submitted by JAMES L SANDRIK
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K970484 |
02/10/1997 |
ACCU-PREP |
BISCO, INC. |
K070583 |
03/01/2007 |
NANO COMPOSITE |
COSMEDENT, INC. |
K060881 |
03/31/2006 |
TEMPORARY CROWN & BRIDGE RESIN |
COSMEDENT, INC. |
K040994 |
04/16/2004 |
COSMEDENT CORE PASTE |
COSMEDENT, INC. |
K961822 |
05/10/1996 |
WET-PREP |
BISCO, INC. |
K041229 |
05/10/2004 |
MULTIPLE (ADDITION SILICONE IMPRESSION MATERIAL) |
COSMEDENT, INC. |
K962946 |
07/29/1996 |
ORTHO-ONE |
BISCO, INC. |
K052263 |
08/19/2005 |
MULTIPLE (TOOTH DESENSITIZER) |
COSMEDENT, INC. |
K092730 |
09/04/2009 |
COSMEDENT BRUSHABLE COMPOSITE |
COSMEDENT, INC. |
K052501 |
09/13/2005 |
MULTIPLE RESIN TOOTH BONDING AGENT |
COSMEDENT, INC. |
K964000 |
10/07/1996 |
BISFIL 2B |
BISCO, INC. |
K042823 |
10/12/2004 |
COSMEDENT PIT & FISSURE SEALANT |
COSMEDENT, INC. |
K974483 |
11/26/1997 |
NTL-FLOW |
BISCO, INC. |
K964931 |
12/10/1996 |
WHITE CORE |
BISCO, INC. |
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