FDA 510(k) Application Details - K102484

Device Classification Name	Device, Percutaneous Retrieval   More FDA Info for this Device
510(K) Number	K102484
Device Name	Device, Percutaneous Retrieval
Applicant	LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. LANGSHAN 2ND STREET NANSHAN DISTRICT SHENZHENG, GUANGDONG 518057 CN Other 510(k) Applications for this Company
Contact	SHI XIAOLI Other 510(k) Applications for this Contact
Regulation Number	870.5150   More FDA Info for this Regulation Number
Classification Product Code	MMX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/2010
Decision Date	11/09/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review