Device Classification Name |
System, Simulation, Radiation Therapy
|
510(k) Number |
K760420 |
Device Name |
FILTER, VACUUM LINE LINEGUARD |
Applicant |
DIEMOLDING CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
DIEMOLDING CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 892.5840
|
Classification Product Code |
|
Date Received | 08/06/1976 |
Decision Date | 08/23/1976 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|