FDA 510(k) Application Details - K162201

Device Classification Name

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510(K) Number K162201
Device Name Desara TV, Desara Blue TV
Applicant CALDERA MEDICAL, INC.
5171 CLARETON DRIVE
Agoura Hills, CA 91301 US
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Contact Vicki Gail
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Regulation Number

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Classification Product Code OTN
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Date Received 08/05/2016
Decision Date 01/11/2017
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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