FDA 510(k) Application Details - K152223

Device Classification Name Chamber, Hyperbaric

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510(K) Number K152223
Device Name Chamber, Hyperbaric
Applicant OXYHEAL MEDICAL SYSTEMS, INC.
3224 HOOVER AVE.
National City, CA 91950 US
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Contact Edward J Chomas
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Regulation Number 868.5470

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Classification Product Code CBF
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Date Received 08/07/2015
Decision Date 04/29/2016
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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