FDA 510(k) Applications Submitted by CHRISTOPHER B LAKE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K051171 |
05/06/2005 |
STINGRAY EPIDURAL CATHETER CONNECTOR |
EPIMED INTERNATIONAL, INC. |
| K051860 |
07/08/2005 |
FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837 |
EPIMED INTERNATIONAL, INC. |
| K053318 |
11/30/2005 |
RX EPIDURAL NEEDLE |
EPIMED INTERNATIONAL, INC. |
| K043467 |
12/15/2004 |
FLEXIBLE SPINAL NEEDLE |
EPIMED INTERNATIONAL, INC. |
| K030562 |
02/21/2003 |
TUOHY EPIDURAL NEEDLE |
EPIMED INTERNATIONAL, INC. |
| K020926 |
03/21/2002 |
EXTENSION SET, MODELS 1911-512 |
EPIMED INTERNATIONAL, INC. |
| K041021 |
04/20/2004 |
RF INTRODUCTION CANNULA |
EPIMED INTERNATIONAL, INC. |
| K022029 |
06/21/2002 |
QUINCKE SPINAL NEEDLE |
EPIMED INTERNATIONAL, INC. |
| K023140 |
09/20/2002 |
VERSA-KATH EPIDURAL CATHETER, MODEL 156-2124 |
EPIMED INTERNATIONAL, INC. |
|
|
