FDA 510(k) Application Details - K140533

Device Classification Name	Surgical Film   More FDA Info for this Device
510(K) Number	K140533
Device Name	Surgical Film
Applicant	TEPHA, INC. 99 HAYDEN, SUTIE 360 LEXINGTON, MA 02421 US Other 510(k) Applications for this Company
Contact	MARY P LEGRAW Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	OOD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2014
Decision Date	05/21/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review