FDA 510(k) Application Details - K990155

Device Classification Name	Cement, Dental   More FDA Info for this Device
510(K) Number	K990155
Device Name	Cement, Dental
Applicant	KAY SEE DENTAL MFG. CO. 124 EAST MISSOURI AVE. KANSAS CITY, MO 64106-1294 US Other 510(k) Applications for this Company
Contact	CLARK SMITH Other 510(k) Applications for this Contact
Regulation Number	872.3275   More FDA Info for this Regulation Number
Classification Product Code	EMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/19/1999
Decision Date	02/25/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review