Device Classification Name |
Syringe, Piston
More FDA Info for this Device |
510(K) Number |
K221308 |
Device Name |
Syringe, Piston |
Applicant |
Jiangxi Maidikang Medical Devices Co., Ltd
Room 308, floor 3, building 1, Jiangxi pharmaceutical co.,
Ltd, No 999, kelun Avenue, pharmaceutical industrial park
Yichun CN
Other 510(k) Applications for this Company
|
Contact |
Wu Huansheng
Other 510(k) Applications for this Contact |
Regulation Number |
880.5860
More FDA Info for this Regulation Number |
Classification Product Code |
FMF
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
05/05/2022 |
Decision Date |
10/17/2022 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
HO - General Hospital |
Review Advisory Committee |
HO - General Hospital |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|