FDA 510(k) Application Details - K972775

Device Classification Name	Dam, Rubber   More FDA Info for this Device
510(K) Number	K972775
Device Name	Dam, Rubber
Applicant	INTERDENT, INC. 2230 SOUTH BARRINGTON LOS ANGELES, CA 90064 US Other 510(k) Applications for this Company
Contact	WILLIAM GRONDIN Other 510(k) Applications for this Contact
Regulation Number	872.6300   More FDA Info for this Regulation Number
Classification Product Code	EIE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/1997
Decision Date	02/27/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review