FDA 510(k) Application Details - K000620

Device Classification Name	System, Intrafallopian Cannula   More FDA Info for this Device
510(K) Number	K000620
Device Name	System, Intrafallopian Cannula
Applicant	MEDICAL DEVICE TECHNOLOGIES, INC. 3600 SW 47TH AVENUE GAINESVILLE, FL 32608 US Other 510(k) Applications for this Company
Contact	KARL SWARTZ Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MDG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/24/2000
Decision Date	10/30/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review