Device Classification Name |
set, administration, intravascular
|
510(k) Number |
K892440 |
Device Name |
KENDALL CURITY EXTENSION TUBES |
Applicant |
THE KENDAL CO. |
ONE FEDERAL ST. |
BOSTON,
MA
02110 -2003
|
|
Applicant Contact |
WILLIAM D CURTIN |
Correspondent |
THE KENDAL CO. |
ONE FEDERAL ST. |
BOSTON,
MA
02110 -2003
|
|
Correspondent Contact |
WILLIAM D CURTIN |
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 04/10/1989 |
Decision Date | 07/24/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|