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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tomography, Optical Coherence
510(k) Number K141844
Device Name RESCAN 700, CALLISTO EYE
Applicant
Carl Zeiss Meditec, AG
5160 Hacienda Dr.
Dublin,  CA  94568
Applicant Contact MANDY AMBRECHT
Correspondent
Carl Zeiss Meditec, AG
5160 Hacienda Dr.
Dublin,  CA  94568
Correspondent Contact MANDY AMBRECHT
Regulation Number886.1570
Classification Product Code
OBO  
Date Received07/08/2014
Decision Date 11/18/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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