Device Classification Name |
Accessory, Assisted Reproduction
|
510(k) Number |
K113075 |
Device Name |
EMBRYO VIEWER SOFTWARE |
Applicant |
UNISENSE FERTILITECH A/S |
TUEAGER 1 |
ARRHUS N,
DK
DK-8200
|
|
Applicant Contact |
METTE MUNCH |
Correspondent |
UNISENSE FERTILITECH A/S |
TUEAGER 1 |
ARRHUS N,
DK
DK-8200
|
|
Correspondent Contact |
METTE MUNCH |
Regulation Number | 884.6120
|
Classification Product Code |
|
Date Received | 10/17/2011 |
Decision Date | 12/21/2011 |
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
|
|
|