FDA 510(k) Application Details - K013053

Device Classification Name	Device, External Penile Rigidity   More FDA Info for this Device
510(K) Number	K013053
Device Name	Device, External Penile Rigidity
Applicant	NANMA MFG CO., LTD. P.O. BOX 4341 CROFTON, MD 21114 US Other 510(k) Applications for this Company
Contact	YOLANDA SMITH Other 510(k) Applications for this Contact
Regulation Number	876.5020   More FDA Info for this Regulation Number
Classification Product Code	LKY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/2001
Decision Date	05/09/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review