FDA 510(k) Application Details - K240959

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K240959
Device Name	Percussor, Powered-Electric
Applicant	Chongqing Moffy Innovation Technology Co.,Ltd. No.292 Jingdongfang Rd.Beibei Dist Chongqing 400714 CN Other 510(k) Applications for this Company
Contact	Yongxu Li Other 510(k) Applications for this Contact
Regulation Number	868.5665   More FDA Info for this Regulation Number
Classification Product Code	BYI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/08/2024
Decision Date	12/18/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review