FDA 510(k) Application Details - K965026

Device Classification Name	Paper, Articulation   More FDA Info for this Device
510(K) Number	K965026
Device Name	Paper, Articulation
Applicant	PFINGST & CO., INC. 105 SNYDER RD. SOUTH PLAINFIELD,, NJ 07080 US Other 510(k) Applications for this Company
Contact	DAVID PFINGST Other 510(k) Applications for this Contact
Regulation Number	872.6140   More FDA Info for this Regulation Number
Classification Product Code	EFH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/17/1996
Decision Date	02/10/1997
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