FDA 510(k) Application Details - K974622

Device Classification Name	Clasp, Preformed   More FDA Info for this Device
510(K) Number	K974622
Device Name	Clasp, Preformed
Applicant	MICRO DENTAL LABORATORIES 6665 AMADOR PLAZA RD., #200 DUBLIN, CA 94568 US Other 510(k) Applications for this Company
Contact	NICOLAS E AZAR Other 510(k) Applications for this Contact
Regulation Number	872.3285   More FDA Info for this Regulation Number
Classification Product Code	EHP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/11/1997
Decision Date	02/10/1998
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