Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K101177
Device Classification Name
Locator, Root Apex
More FDA Info for this Device
510(K) Number
K101177
Device Name
Locator, Root Apex
Applicant
MEDICNRG LTD.
291 HILLSIDE AVE.
SOMERSET, MA 02726 US
Other 510(k) Applications for this Company
Contact
George Hattub
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
04/27/2010
Decision Date
10/08/2010
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