FDA 510(k) Applications Submitted by THOMAS MEDICAL PRODUCTS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K004025 |
12/27/2000 |
SPLITTABLE SHEATH INTRODUCER KIT |
THOMAS MEDICAL PRODUCTS, INC. |
| K003731 |
12/04/2000 |
SAFESHEATH MSP INTRODUCER SHEATH KIT WITH INTEGRAL HEMOSTASIS VALVE |
THOMAS MEDICAL PRODUCTS, INC. |
| K004026 |
12/27/2000 |
BRAIDED GUIDING INTRODUCER |
THOMAS MEDICAL PRODUCTS, INC. |
| K961466 |
04/17/1996 |
PERCUTANEOUS INTRODUCER SET |
THOMAS MEDICAL PRODUCTS, INC. |
| K961780 |
05/08/1996 |
HEMODIALYSIS INTRODUCER SET |
THOMAS MEDICAL PRODUCTS, INC. |
| 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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