FDA 510(k) Application Details - K152436

Device Classification Name	Booth, Sun Tan   More FDA Info for this Device
510(K) Number	K152436
Device Name	Booth, Sun Tan
Applicant	Interlectric Corporation 1401 Lexington Ave. Warren, PA 16365 US Other 510(k) Applications for this Company
Contact	Ken C. Frazier Other 510(k) Applications for this Contact
Regulation Number	878.4635   More FDA Info for this Regulation Number
Classification Product Code	LEJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/2015
Decision Date	12/07/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review