FDA 510(k) Application Details - K002912

Device Classification Name	Speculum, Vaginal, Nonmetal   More FDA Info for this Device
510(K) Number	K002912
Device Name	Speculum, Vaginal, Nonmetal
Applicant	STERINC 3520 W. WARNER AVE. SANTA ANTA, CA 92704 US Other 510(k) Applications for this Company
Contact	TODD ABRAHAM Other 510(k) Applications for this Contact
Regulation Number	884.4530   More FDA Info for this Regulation Number
Classification Product Code	HIB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/18/2000
Decision Date	02/21/2001
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