Device Classification Name |
system, abortion, vacuum
|
510(k) Number |
K840384 |
Device Name |
DIAGNOSTIC DILATATION & MENSTRUAL KIT |
Applicant |
INTL. MEDICAL TECHNOLOGIES, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
INTL. MEDICAL TECHNOLOGIES, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 884.5070
|
Classification Product Code |
|
Date Received | 01/30/1984 |
Decision Date | 04/30/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|