Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K210877
Device Classification Name
More FDA Info for this Device
510(K) Number
K210877
Device Name
Evolve System with the T3 Applicator
Applicant
InMode Ltd.
Tabor Building, Shaar Yokneam
Yoqneam Illit 2069200 IL
Other 510(k) Applications for this Company
Contact
Amit Goren
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
PBX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/24/2021
Decision Date
07/19/2021
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact