FDA 510(k) Application Details - K973800

Device Classification Name	Handpiece, Contra- And Right-Angle Attachment, Dental   More FDA Info for this Device
510(K) Number	K973800
Device Name	Handpiece, Contra- And Right-Angle Attachment, Dental
Applicant	MIDWEST DENTAL PRODUCTS CORP. 901 WEST OAKTON ST. DES PLAINES, IL 60018 US Other 510(k) Applications for this Company
Contact	ROBERT E BOOTH Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EGS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/06/1997
Decision Date	03/11/1998
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