Device Classification Name |
Catheter, Conduction, Anesthetic
|
510(k) Number |
K850439 |
Device Name |
DESERET EPIDURAL CATHETER |
Applicant |
PARKE-DAVIS CO. |
870 PARKDALE RD. |
ROCHESTER,
MI
48307
|
|
Applicant Contact |
CLEARY |
Correspondent |
PARKE-DAVIS CO. |
870 PARKDALE RD. |
ROCHESTER,
MI
48307
|
|
Correspondent Contact |
CLEARY |
Regulation Number | 868.5120
|
Classification Product Code |
|
Date Received | 02/05/1985 |
Decision Date | 03/05/1985 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|