Device Classification Name |
Anesthesia Conduction Kit
|
510(k) Number |
K033952 |
Device Name |
PERIFIX CATHETER CONNECTOR |
Applicant |
B. BRAUN MEDICAL, INC. |
901 MARCON BLVD. |
ALLENTOWN,
PA
18109 -9341
|
|
Applicant Contact |
AMY SMITH |
Correspondent |
B. BRAUN MEDICAL, INC. |
901 MARCON BLVD. |
ALLENTOWN,
PA
18109 -9341
|
|
Correspondent Contact |
AMY SMITH |
Regulation Number | 868.5140
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 12/22/2003 |
Decision Date | 02/04/2004 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|