FDA 510(k) Application Details - K980216

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K980216
Device Name	Airbrush
Applicant	KREATIV, INC. 1517 INDUSTRIAL WAY, S.W. ALBANY, OR 97321 US Other 510(k) Applications for this Company
Contact	JOE FOREHAND 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	01/21/1998
Decision Date	06/16/1998
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