Device Classification Name |
Catheter, Conduction, Anesthetic
|
510(k) Number |
K991879 |
Device Name |
SPRING-WOUND EPIDURAL CATHETER |
Applicant |
MICOR, INC. |
2855 OXFORD BLVD. |
ALLISON PARK,
PA
15101
|
|
Applicant Contact |
CHARLES W ESLEEP |
Correspondent |
MICOR, INC. |
2855 OXFORD BLVD. |
ALLISON PARK,
PA
15101
|
|
Correspondent Contact |
CHARLES W ESLEEP |
Regulation Number | 868.5120
|
Classification Product Code |
|
Date Received | 06/02/1999 |
Decision Date | 10/28/1999 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|