Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K210093
Device Classification Name
More FDA Info for this Device
510(K) Number
K210093
Device Name
AccuFFRangio
Applicant
ArteryFlow Technology Co., Ltd.
459 Qianmo Road, Suite C1-501, Binjiang District
Hangzhou 310051 CN
Other 510(k) Applications for this Company
Contact
Jianping Xiang
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
QHA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/14/2021
Decision Date
09/10/2021
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact