Device Classification Name |
Endoscope, Flexible
|
510(k) Number |
K900894 |
Device Name |
MEDILASE SERIES 2100 ENDOSCOPE |
Applicant |
MEDICAL LASER, INC. |
2605 FERNBROOK LN. |
MINNEAPOLIS,
MN
55447
|
|
Applicant Contact |
SHARON KARR |
Correspondent |
MEDICAL LASER, INC. |
2605 FERNBROOK LN. |
MINNEAPOLIS,
MN
55447
|
|
Correspondent Contact |
SHARON KARR |
Regulation Number | 876.1500
|
Classification Product Code |
|
Date Received | 02/27/1990 |
Decision Date | 06/22/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|