Device Classification Name |
instrument, surgical, disposable
|
510(k) Number |
K803156 |
Device Name |
SURGITEK MEDI-LOOPS |
Applicant |
MEDICAL ENGINEERING CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
MEDICAL ENGINEERING CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.4800
|
Classification Product Code |
|
Date Received | 12/12/1980 |
Decision Date | 01/15/1981 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|