FDA 510(k) Application Details - K950259

Device Classification Name	Attachment, Precision, All   More FDA Info for this Device
510(K) Number	K950259
Device Name	Attachment, Precision, All
Applicant	DR. JOSEPH E. GRASSO, D.D.S. 4 ROSWELL RD. WEST SIMSBURY, CT 06092 US Other 510(k) Applications for this Company
Contact	JOSEPH E GRASSO Other 510(k) Applications for this Contact
Regulation Number	872.3165   More FDA Info for this Regulation Number
Classification Product Code	EGG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/23/1995
Decision Date	12/06/1996
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