Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K171867
Device Classification Name
Locator, Root Apex
More FDA Info for this Device
510(K) Number
K171867
Device Name
Locator, Root Apex
Applicant
Good Doctors Co.,Ltd.
#208, B-Dong, 283 Bupyeong-Daero, Bupyeong-Gu
Incheon 21315 KR
Other 510(k) Applications for this Company
Contact
Sungro Joo
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LQY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/22/2017
Decision Date
03/30/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact