Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K222206
Device Classification Name
Massager, Powered Inflatable Tube
More FDA Info for this Device
510(K) Number
K222206
Device Name
Massager, Powered Inflatable Tube
Applicant
Shenzhen Dongjilian Medical Tech Co., Ltd.
B1/15F, Tonglu Industrial Area, Tongxin Community,
Longgang District
Shenzhen 518116 CN
Other 510(k) Applications for this Company
Contact
Zhang Hong
Other 510(k) Applications for this Contact
Regulation Number
890.5650
More FDA Info for this Regulation Number
Classification Product Code
IRP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/25/2022
Decision Date
09/30/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact