Device Classification Name |
Electrode, Electrosurgical, Active, Urological
|
510(k) Number |
K903162 |
Device Name |
FLEXIBLE ENDOSCOPIC ELECTRODES |
Applicant |
NORTH AMERICAN STERILIZATION & PACKAGING CO. |
15 WHITE LAKE RD. |
P.O. BOX 923 |
SPARTA,
NJ
07871
|
|
Applicant Contact |
HARRY SCHLAKMAN |
Correspondent |
NORTH AMERICAN STERILIZATION & PACKAGING CO. |
15 WHITE LAKE RD. |
P.O. BOX 923 |
SPARTA,
NJ
07871
|
|
Correspondent Contact |
HARRY SCHLAKMAN |
Regulation Number | 876.4300
|
Classification Product Code |
|
Date Received | 07/18/1990 |
Decision Date | 12/18/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|