FDA 510(k) Application Details - K102859

Device Classification Name Camera, Ophthalmic, Ac-Powered

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510(K) Number K102859
Device Name Camera, Ophthalmic, Ac-Powered
Applicant CLARITY MEDICAL SYSTEMS
5775 WEST LAS POSITAS BLVD.
SUITE 200
PLEASANTON, CA 94588-4084 US
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Contact GARY A SEEGER
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Regulation Number 886.1120

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Classification Product Code HKI
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Date Received 09/30/2010
Decision Date 04/20/2011
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



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