FDA 510(k) Application Details - K970484

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K970484
Device Name	Airbrush
Applicant	BISCO, INC. 1500 W. THORNDALE AVE. ITASCA, IL 60143 US Other 510(k) Applications for this Company
Contact	JAMES L SANDRIK 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	02/10/1997
Decision Date	07/01/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review