Device Classification Name |
anesthesia conduction kit
|
510(k) Number |
K801912 |
Device Name |
ARROW POSITIVE PLACEMENT CON/EPIDURAL AN |
Applicant |
ARROW INTL., INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
ARROW INTL., INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 868.5140
|
Classification Product Code |
|
Date Received | 08/11/1980 |
Decision Date | 09/16/1980 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|