Device Classification Name |
cannula, manipulator/injector, uterine
|
510(k) Number |
K961752 |
Device Name |
H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607) |
Applicant |
ACKRAD LABORATORIES |
70 JACKSON DR. |
CRANFORD,
NJ
07016
|
|
Applicant Contact |
BERNARD ACKERMAN |
Correspondent |
ACKRAD LABORATORIES |
70 JACKSON DR. |
CRANFORD,
NJ
07016
|
|
Correspondent Contact |
BERNARD ACKERMAN |
Regulation Number | 884.4530
|
Classification Product Code |
|
Date Received | 05/06/1996 |
Decision Date | 08/08/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|