FDA 510(k) Application Details - K133217

Device Classification Name	Tomography, Optical Coherence   More FDA Info for this Device
510(K) Number	K133217
Device Name	Tomography, Optical Coherence
Applicant	CARL ZEISS MEDITEC AG 5160 HACIENDA DRIVE DUBLIN, CA 94568 US Other 510(k) Applications for this Company
Contact	MANDY AMBRECHT Other 510(k) Applications for this Contact
Regulation Number	886.1570   More FDA Info for this Regulation Number
Classification Product Code	OBO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/18/2013
Decision Date	03/19/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review