FDA 510(k) Application Details - K974752

Device Classification Name	Barrier, Synthetic, Intraoral   More FDA Info for this Device
510(K) Number	K974752
Device Name	Barrier, Synthetic, Intraoral
Applicant	IMTEC CORP. 2401 NORTH COMMERCE ARDMORE, OK 73401 US Other 510(k) Applications for this Company
Contact	M. K. PATTERSON Other 510(k) Applications for this Contact
Regulation Number	872.3930   More FDA Info for this Regulation Number
Classification Product Code	NPK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/19/1997
Decision Date	03/03/1998
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