Device Classification Name |
needle, hypodermic, single lumen
|
510(k) Number |
K070440 |
Device Name |
BD HYPOINT NEEDLE |
Applicant |
BECTON DICKINSON & CO. |
1 BECTON DR. |
FRANKLIN LAKES,
NJ
07417 -1880
|
|
Applicant Contact |
AILEEN C GILBERT |
Correspondent |
BECTON DICKINSON & CO. |
1 BECTON DR. |
FRANKLIN LAKES,
NJ
07417 -1880
|
|
Correspondent Contact |
AILEEN C GILBERT |
Regulation Number | 880.5570
|
Classification Product Code |
|
Date Received | 02/15/2007 |
Decision Date | 03/16/2007 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|