FDA 510(k) Applications Submitted by BENJAMIN LICHTENWALNER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K100273 |
01/29/2010 |
INSTAFLO BOWEL CATHETER SYSTEM KIT |
HOLLISTER, INC. |
K050647 |
03/14/2005 |
ALL-IN-ONE |
BISCO, INC. |
K060701 |
03/16/2006 |
BISCEM TRANSLUCENT, BISCEM OPAQUE |
BISCO, INC. |
K051999 |
07/25/2005 |
BISCOVER LED |
BISCO, INC. |
K052122 |
08/05/2005 |
BISCO LED |
BISCO, INC. |
K042804 |
10/12/2004 |
TESCERA OPAQUER POWDER/SCULPTING RESIN |
BISCO, INC. |
K063237 |
10/26/2006 |
THERACAL LC |
BISCO, INC. |
K033472 |
11/03/2003 |
TESCERA U-BAR AND BARRELS |
BISCO, INC. |
K033521 |
11/07/2003 |
BISBLOCK |
BISCO, INC. |
K033551 |
11/10/2003 |
EVOLVE |
RELIANCE ORTHODONTIC PRODUCTS, INC. |
K033585 |
11/13/2003 |
DIAPEX |
BISCO, INC. |
K043168 |
11/16/2004 |
BISCOVER LV |
BISCO, INC. |
K073263 |
11/20/2007 |
PRO-V |
BISCO, INC. |
K063780 |
12/21/2006 |
ACE BOND SE |
BISCO, INC. |
K034024 |
12/29/2003 |
TESCERA FIBER BUNDLES, FIBER MESH AND FIBER CYLINDERS |
BISCO, INC. |
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