Device Classification Name |
system, measurement, blood-pressure, non-invasive
|
510(k) Number |
K031327 |
Device Name |
VERICOR |
Applicant |
CVP DIAGNOSTICS, INC. |
2305 GOLD MINE RD. |
BROOKEVILLE,
MD
20833
|
|
Applicant Contact |
T. WHIT ATHEY |
Correspondent |
CVP DIAGNOSTICS, INC. |
2305 GOLD MINE RD. |
BROOKEVILLE,
MD
20833
|
|
Correspondent Contact |
T. WHIT ATHEY |
Regulation Number | 870.1130
|
Classification Product Code |
|
Date Received | 04/25/2003 |
Decision Date | 05/12/2004 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|