Device Classification Name |
Syringe, Piston
|
510(k) Number |
K172670 |
Device Name |
BD Single Use, Hypodermic Syringe |
Applicant |
Becton, Dickinson and Company |
1 Becton Drive |
Franklin Lakes,
NJ
07417
|
|
Applicant Contact |
Victoria Morrow |
Correspondent |
Becton, Dickinson and Company |
1 Becton Drive |
Franklin Lakes,
NJ
07417
|
|
Correspondent Contact |
Victoria Morrow |
Regulation Number | 880.5860
|
Classification Product Code |
|
Date Received | 09/05/2017 |
Decision Date | 10/23/2018 |
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
|
|
|