FDA 510(k) Application Details - K002329

Device Classification Name	Pessary, Vaginal   More FDA Info for this Device
510(K) Number	K002329
Device Name	Pessary, Vaginal
Applicant	DESCHUTES MEDICAL PRODUCTS, INC. 1011 S.W. EMKAY DR., SUITE 104 BEND, OR 97702 US Other 510(k) Applications for this Company
Contact	DENISE BESTWICK Other 510(k) Applications for this Contact
Regulation Number	884.3575   More FDA Info for this Regulation Number
Classification Product Code	HHW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/01/2000
Decision Date	09/18/2000
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