Device Classification Name |
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
|
510(k) Number |
K860290 |
Device Name |
VIAPIC CENTRAL LINE CATHETER |
Applicant |
PARKE-DAVIS CO. |
870 PARKDALE RD. |
ROCHESTER,
MI
48307
|
|
Applicant Contact |
E. F CLEARY |
Correspondent |
PARKE-DAVIS CO. |
870 PARKDALE RD. |
ROCHESTER,
MI
48307
|
|
Correspondent Contact |
E. F CLEARY |
Regulation Number | 880.5200
|
Classification Product Code |
|
Date Received | 01/28/1986 |
Decision Date | 03/18/1986 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|