Device Classification Name |
oxygenator, cardiopulmonary bypass
|
510(k) Number |
K130520 |
Device Name |
CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR |
Applicant |
ASHITAKA FACTORY OF TERUMO CORP. |
150 MAIMAIGI-CHO |
FUJINOMIYA, SHIZUOKA,
JP
418-0015
|
|
Applicant Contact |
EILEEN DORSEY |
Correspondent |
ASHITAKA FACTORY OF TERUMO CORP. |
150 MAIMAIGI-CHO |
FUJINOMIYA, SHIZUOKA,
JP
418-0015
|
|
Correspondent Contact |
EILEEN DORSEY |
Regulation Number | 870.4350
|
Classification Product Code |
|
Date Received | 02/28/2013 |
Decision Date | 03/13/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
Yes
|
|
|