Device Classification Name |
Anesthesia Conduction Kit
|
510(k) Number |
K880970 |
Device Name |
AXILLARY BLOCK NEEDLE |
Applicant |
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC |
1 BECTON DR. |
FRANKLIN LAKES,
NJ
07417 -1880
|
|
Applicant Contact |
RUSSELL ARNSBERGER |
Correspondent |
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC |
1 BECTON DR. |
FRANKLIN LAKES,
NJ
07417 -1880
|
|
Correspondent Contact |
RUSSELL ARNSBERGER |
Regulation Number | 868.5140
|
Classification Product Code |
|
Date Received | 03/08/1988 |
Decision Date | 04/21/1988 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|