FDA 510(k) Application Details - K964755

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K964755
Device Name	Airbrush
Applicant	MIDWEST DENTAL PRODUCTS CORP. 901 WEST OAKTON ST. DES PLAINES, IL 60018 US Other 510(k) Applications for this Company
Contact	HECTOR JIMENEZ-BILLINI Other 510(k) Applications for this Contact
Regulation Number	872.6080   More FDA Info for this Regulation Number
Classification Product Code	KOJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/27/1996
Decision Date	09/11/1997
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