FDA 510(k) Application Details - K000117

Device Classification Name	Set, Anesthesia, Paracervical   More FDA Info for this Device
510(K) Number	K000117
Device Name	Set, Anesthesia, Paracervical
Applicant	AVID MEDICAL, INC. 9000 WESTMONT DR. STONEHOUSE COMMERCE PARK TOANO, VA 23168 US Other 510(k) Applications for this Company
Contact	SEAN F SHEMANSKI Other 510(k) Applications for this Contact
Regulation Number	884.5100   More FDA Info for this Regulation Number
Classification Product Code	HEE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/14/2000
Decision Date	04/13/2000
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