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FDA 510(k) Applications Submitted by MANDY AMBRECHT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130648
03/11/2013
FORUM GLAUCOMA WORKPLACE
CARL ZEISS MEDITEC AG
K150977
04/13/2015
CIRRUS HD-OCT
CARL ZEISS MEDITEC INC
K141297
05/19/2014
FORUM GLAUCOMA WORKPLACE
CARL ZEISS MEDITEC AG
K181534
06/11/2018
CIRRUS HD-OCT
Carl Zeiss Meditec, Inc.
K141844
07/08/2014
RESCAN 700, CALLISTO EYE
CARL ZEISS MEDITEC AG
K133217
10/18/2013
CIRRUS PHOTO
CARL ZEISS MEDITEC AG
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