FDA 510(k) Applications Submitted by BREG, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K961855 |
05/14/1996 |
POLAR CARE (MODEL 500/50000) |
BREG, INC. |
| 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. |
|
|
