FDA 510(k) Application Details - K131373

Device Classification Name	Clamp, Circumcision   More FDA Info for this Device
510(K) Number	K131373
Device Name	Clamp, Circumcision
Applicant	WUHU SNNDA MEDICAL TREATMENT APPLIANCE TECHNOLOGY 503 ROOM, 8 BUILDING, 600 LIU ZHOU ROAD SHANGHAI 200233 CN Other 510(k) Applications for this Company
Contact	BO GONG Other 510(k) Applications for this Contact
Regulation Number	884.4530   More FDA Info for this Regulation Number
Classification Product Code	HFX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/13/2013
Decision Date	06/25/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review