Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by CIMILRE CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162870
10/13/2016
CIMLRE F1 and CIMILRE S3
CIMILRE CO., LTD.
K221708
06/13/2022
CIMILRE Free-T2 Plus
Cimilre Co., Ltd.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact