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
K093537
11/16/2009
HANAROSTENT ESOPHAGUS (CCC)
M.I. TECH CO., LTD.
K072094
07/30/2007
CHOOSTENT
M.I. TECH CO., LTD.
K180180
01/23/2018
HANAROSTENT LowAxTM Colon/Rectum (NNN), HANAROSTENT LowAxTM Duodenum/Pylorus (NNN)
M.I. Tech Co., Ltd.
K201342
05/20/2020
HANAROSTENT Trachea/Bronchium (CCC)
M.I. Tech Co., Ltd.
K183616
12/26/2018
HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN)
M.I. Tech Co., Ltd.
K111149
04/25/2011
HANAROSTENT BILIARY (NNN)
M.I. TECH CO., LTD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact