Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K220268
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K220268
Device Name
Powered Laser Surgical Instrument
Applicant
Beijing ADSS Development Co., Ltd.
F2,Building 1,Jinyuan Road 36 Daxing Economic Development
Zone
Beijing 102628 CN
Other 510(k) Applications for this Company
Contact
Song Ying
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/31/2022
Decision Date
08/23/2022
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