Device Classification Name |
forceps
|
510(k) Number |
K840766 |
Device Name |
JANACEK TUBO-UTERINE IMPLANTATION SET |
Applicant |
CIMED INTL., INC. |
C/O MYRON E. SILDON ASSOCIATES |
2800 CITY CTR SQ./1100 MAIN ST |
KANSAS CITY ,
MO
64105 -
|
|
Applicant Contact |
JAMES L KENWORTHY |
Correspondent |
CIMED INTL., INC. |
C/O MYRON E. SILDON ASSOCIATES |
2800 CITY CTR SQ./1100 MAIN ST |
KANSAS CITY ,
MO
64105 -
|
|
Correspondent Contact |
JAMES L KENWORTHY |
Regulation Number | 878.4800
|
Classification Product Code |
|
Date Received | 02/23/1984 |
Decision Date | 04/23/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|