FDA 510(k) Application Details - K030292

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K030292
Device Name	Airbrush
Applicant	GROMAN INC. 1917 NW 80 AVE. MARGATE, FL 33063 US Other 510(k) Applications for this Company
Contact	BARRY B GROMAN 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	01/28/2003
Decision Date	04/15/2003
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