Device Classification Name |
Laparoscope, Gynecologic (And Accessories)
|
510(k) Number |
K062097 |
Device Name |
VERESS CANNULA AND MODULAR VERESS CANNULA |
Applicant |
PAJUNK GMBH MEDIZINTECHNOLOGIE |
KARL-HALL-STRASSE 1 |
GEISINGEN, BADEN-WURTTEMBERG,
DE
78187
|
|
Applicant Contact |
CHRISTIAN QUASS |
Correspondent |
PAJUNK GMBH MEDIZINTECHNOLOGIE |
KARL-HALL-STRASSE 1 |
GEISINGEN, BADEN-WURTTEMBERG,
DE
78187
|
|
Correspondent Contact |
CHRISTIAN QUASS |
Regulation Number | 884.1720
|
Classification Product Code |
|
Date Received | 07/24/2006 |
Decision Date | 10/13/2006 |
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
|
|
|