FDA 510(k) Application Details - K032887

Device Classification Name	Media, Reproductive   More FDA Info for this Device
510(K) Number	K032887
Device Name	Media, Reproductive
Applicant	IRVINE SCIENTIFIC SALES CO., INC. 2511 DAIMLER ST. SANTA ANA, CA 92705 US Other 510(k) Applications for this Company
Contact	WENDELL LEE Other 510(k) Applications for this Contact
Regulation Number	884.6180   More FDA Info for this Regulation Number
Classification Product Code	MQL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/2003
Decision Date	12/19/2003
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