Device Classification Name |
set, administration, intravascular
|
510(k) Number |
K854804 |
Device Name |
MULTIPLE I.V. SETS |
Applicant |
C. B. DUMONT COMPANY, INC. |
P.O. BOX 418 |
NEWPORT,
RI
02840
|
|
Applicant Contact |
BERTRAND DUMONT |
Correspondent |
C. B. DUMONT COMPANY, INC. |
P.O. BOX 418 |
NEWPORT,
RI
02840
|
|
Correspondent Contact |
BERTRAND DUMONT |
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 12/02/1985 |
Decision Date | 02/12/1986 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|