FDA 510(k) Application Details - K111201

Device Classification Name	System, Imaging, Optical Coherence Tomography (Oct)   More FDA Info for this Device
510(K) Number	K111201
Device Name	System, Imaging, Optical Coherence Tomography (Oct)
Applicant	LIGHTLAB IMAGING,INC. ONE TECHNOLOGY PARK DRIVE WESTFORD, MA 01886 US Other 510(k) Applications for this Company
Contact	BRYAN COWELL Other 510(k) Applications for this Contact
Regulation Number	892.1560   More FDA Info for this Regulation Number
Classification Product Code	NQQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/29/2011
Decision Date	08/10/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review