FDA 510(k) Applications Submitted by KATHLEEN BARBER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K070402 |
02/12/2007 |
MODIFICATION TO POLAR CARE 500 |
BREG, INC. |
K020988 |
03/27/2002 |
PAIN CARE 4200 |
BREG, INC. |
K041714 |
06/23/2004 |
E-PAIN CARE |
BREG, INC. |
K002073 |
07/10/2000 |
PAIN CARE 3000 |
BREG, INC. |
K002321 |
07/31/2000 |
PAIN CARE 2000L |
BREG, INC. |
K963596 |
09/09/1996 |
POLAR CARE 300 |
BREG, INC. |
K983454 |
09/30/1998 |
PAIN CARE 2000 |
BREG, INC. |
K003611 |
11/22/2000 |
PAIN CARE MULTI-PORT CATHETER, MODEL 2000L |
BREG, INC. |
K013928 |
11/28/2001 |
PAIN CARE 3200 |
BREG, INC. |
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