FDA 510(k) Application Details - K153239

Device Classification Name Camera, Ophthalmic, Ac-Powered

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510(K) Number K153239
Device Name Camera, Ophthalmic, Ac-Powered
Applicant Softcare Co., Ltd
243-5 Yatsunami
Fukutsu 811-3201 JP
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Contact Noriyoshi Takahashi
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Regulation Number 886.1120

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Classification Product Code HKI
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Date Received 11/09/2015
Decision Date 05/12/2016
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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