FDA 510(k) Application Details - K041028

Device Classification Name	Material, Impression   More FDA Info for this Device
510(K) Number	K041028
Device Name	Material, Impression
Applicant	CROWN DELTA CORP. 1550 FRONT ST. YORKTOWN HEIGHTS, NY 10598 US Other 510(k) Applications for this Company
Contact	MARK P KONOPKA Other 510(k) Applications for this Contact
Regulation Number	872.3660   More FDA Info for this Regulation Number
Classification Product Code	ELW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/21/2004
Decision Date	05/14/2004
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