Device Classification Name |
set, administration, intravascular
|
510(k) Number |
K072576 |
Device Name |
CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED |
Applicant |
BAXTER HEALTHCARE CORP. |
1620 WAUKEGAN RD. |
MPGR-AL |
MCGAW PARK,
IL
60085
|
|
Applicant Contact |
NANETTE HEDDEN |
Correspondent |
BAXTER HEALTHCARE CORP. |
1620 WAUKEGAN RD. |
MPGR-AL |
MCGAW PARK,
IL
60085
|
|
Correspondent Contact |
NANETTE HEDDEN |
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 09/13/2007 |
Decision Date | 11/06/2007 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|