Device Classification Name |
set, administration, intravascular
|
510(k) Number |
K001106 |
Device Name |
MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000 |
Applicant |
CREATIVE PLASTIC TECHNOLOGY |
24312 ARMADA DR. |
DANA POINT,
CA
92629
|
|
Applicant Contact |
ROBERT J BARD |
Correspondent |
CREATIVE PLASTIC TECHNOLOGY |
24312 ARMADA DR. |
DANA POINT,
CA
92629
|
|
Correspondent Contact |
ROBERT J BARD |
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 04/05/2000 |
Decision Date | 08/16/2000 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|