FDA 510(k) Application Details - K993953

Device Classification Name	Cap, Cervical   More FDA Info for this Device
510(K) Number	K993953
Device Name	Cap, Cervical
Applicant	VEOS LTD. 273 MARKET SQUARE CT., #12 LAKE FOREST, IL 60045 US Other 510(k) Applications for this Company
Contact	PEGGY S DANNENBAUM Other 510(k) Applications for this Contact
Regulation Number	884.5250   More FDA Info for this Regulation Number
Classification Product Code	HDR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/22/1999
Decision Date	03/21/2000
Decision	SESU - SE - WITH LIMITATIONS
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