Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by M.I.Tech Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190141
01/29/2019
HANAROSTENT LowAx Colon/Rectum (NNN)
M.I.Tech Co., Ltd.
K202973
09/30/2020
HANAROSTENT Benefit Biliary (NNN)
M.I.Tech Co., Ltd.
K183396
12/07/2018
HANAROSTENT FASTTM Biliary (NNN)
M.I.Tech Co., Ltd.
K213251
09/30/2021
HANAROSTENT Esophagus Asymmetric (CCC)
M.I.Tech Co., Ltd.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact