FDA 510(k) Application Details - K962379

Device Classification Name	Stimulator, Electrical For Sperm Collection   More FDA Info for this Device
510(K) Number	K962379
Device Name	Stimulator, Electrical For Sperm Collection
Applicant	NATIONAL REHAB HOSPITAL 102 IRVING STREET, N.W. WASHINGTON, DC 20010-2949 US Other 510(k) Applications for this Company
Contact	S.W.J. SEAGER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LNL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/1996
Decision Date	09/18/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review