FDA 510(k) Applications Submitted by STEPHEN C SMITH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030585 |
02/24/2003 |
SCULPTING RESIN |
BISCO, INC. |
K024046 |
12/06/2002 |
TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P |
BISCO, INC. |
K030951 |
03/26/2003 |
TESCERAFLO A2, MODEL T-21012P; TESCERAFLO A2 OPAQUE, MODEL T-210120P |
BISCO, INC. |
K021503 |
05/09/2002 |
UNINHIBITED |
BISCO, INC. |
K110255 |
01/28/2011 |
SOUND SURGICAL TECHNOLOGIES LLC POWERX LIPO SYSTEM |
SOUND SURGICAL TECHNOLOGIES LLC. |
K110306 |
02/02/2011 |
SOUND SURGICAL VASER 2.1 LIPO SYSTEM |
SOUND SURGICAL TECHNOLOGIES LLC. |
K120328 |
02/02/2012 |
ORIGINS LIPOHARVESTING SYSTEM |
SOUND SURGICAL TECHNOLOGIES LLC. |
K030354 |
02/03/2003 |
BISCOVER LIQUID POLISH KIT, BISCOVER LIQUID POLISH AND BISCOVER VISCOSITY MODIFIER |
BISCO, INC. |
K962612 |
07/03/1996 |
BILIBED PHOTOTHERAPY LAMP |
MEDELA, INC. |
K983552 |
10/09/1998 |
BASIC, MEDIAN, DOMINANT, AND VARIO |
MEDELA, INC. |
K013519 |
10/23/2001 |
SIMPLE |
BISCO, INC. |
K984589 |
12/24/1998 |
PHOTOTHERAPY LAMP |
MEDELA, INC. |
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