FDA 510(k) Application Details - K993124

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K993124
Device Name	Airbrush
Applicant	KIS PRODUCTS 2318 SEA ISLAND DR. FT. LAUDERDALE, FL 33301 US Other 510(k) Applications for this Company
Contact	REUBEN HERTZ 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	09/20/1999
Decision Date	08/06/2001
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