Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by KITAZATO MEDICAL CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112396
08/19/2011
IUI CATHETERS
KITAZATO MEDICAL CO., LTD.
K112462
08/26/2011
KITAZATO OPU NEEDLE
KITAZATO MEDICAL CO., LTD.
K131491
05/23/2013
KITAZATO IUI CATHETER
KITAZATO MEDICAL CO., LTD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact