Device Classification Name |
anesthesia conduction kit
|
510(k) Number |
K832778 |
Device Name |
EPIDURAL SYRINGE |
Applicant |
CONCORD LABORATORIES, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
CONCORD LABORATORIES, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 868.5140
|
Classification Product Code |
|
Date Received | 08/16/1983 |
Decision Date | 09/26/1983 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|