Device Classification Name |
implantable pacemaker pulse-generator
|
510(k) Number |
K821033 |
Device Name |
CORATOMIC MODEL OVALITH-920 |
Applicant |
CORATOMIC, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
CORATOMIC, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 870.3610
|
Classification Product Code |
|
Date Received | 04/13/1982 |
Decision Date | 05/28/1982 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|