FDA 510(k) Applications Submitted by TIM STOUDT
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K020090 |
01/10/2002 |
MODIFICATION TO TRANSSEPTAL INTRODUCER SET |
THOMAS MEDICAL PRODUCTS, INC. |
K120158 |
01/18/2012 |
CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITS |
THOMAS MEDICAL PRODUCTS, INC. |
K040713 |
03/18/2004 |
MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEM |
THOMAS MEDICAL PRODUCTS, INC. |
K101015 |
04/12/2010 |
GUIDE CATHETERS AND ACCESSORIES |
THOMAS MEDICAL PRODUCTS, INC. |
K081341 |
05/13/2008 |
REINFORCED CATHETER INTRODUCER SYSTEM (RCIS) |
THOMAS MEDICAL PRODUCTS, INC. |
K011727 |
06/04/2001 |
TRANSSEPTAL NEEDLE/TROCAR |
THOMAS MEDICAL PRODUCTS, INC. |
K122431 |
08/10/2012 |
HEARTSPAN STEERABLE INTRODUCER KIT |
THOMAS MEDICAL PRODUCTS, INC. |
K013202 |
09/25/2001 |
MODIFICATION TO BRAIDED GUIDING INTRODUCER |
THOMAS MEDICAL PRODUCTS, INC. |
K072745 |
09/27/2007 |
Y-GLIDE |
THOMAS MEDICAL PRODUCTS, INC. |
K083269 |
11/05/2008 |
CROSSOVER |
THOMAS MEDICAL PRODUCTS, INC. |
K043438 |
12/14/2004 |
LARGE BORE SPLITTABLE INTRODUCER KIT |
THOMAS MEDICAL PRODUCTS, INC. |
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