FDA 510(k) Application Details - K974117

Device Classification Name	Pessary, Vaginal   More FDA Info for this Device
510(K) Number	K974117
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	MATTHEW W HOSKINS 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	10/31/1997
Decision Date	04/27/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review