FDA 510(k) Application Details - K022025

Device Classification Name	Liner, Cavity, Calcium Hydroxide   More FDA Info for this Device
510(K) Number	K022025
Device Name	Liner, Cavity, Calcium Hydroxide
Applicant	MILTON HODOSH, M.D. 243 ELWOOD AVE. PROVIDENCE, RI 02907 US Other 510(k) Applications for this Company
Contact	MILTON HODOSH Other 510(k) Applications for this Contact
Regulation Number	872.3250   More FDA Info for this Regulation Number
Classification Product Code	EJK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2002
Decision Date	08/15/2002
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