Device Classification Name |
Shunt, Central Nervous System And Components
|
510(k) Number |
K930222 |
Device Name |
CAMINO VENTRICULAR ACCESS DEVICE |
Applicant |
CAMINO LABORATORIES, INC. |
5955 PACIFIC CENTER BLVD. |
SAN DIEGO,
CA
92121
|
|
Applicant Contact |
HAZEL M AKER |
Correspondent |
CAMINO LABORATORIES, INC. |
5955 PACIFIC CENTER BLVD. |
SAN DIEGO,
CA
92121
|
|
Correspondent Contact |
HAZEL M AKER |
Regulation Number | 882.5550
|
Classification Product Code |
|
Date Received | 01/15/1993 |
Decision Date | 04/15/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|