FDA 510(k) Application Details - K212928

Device Classification Name Barrier,Std,Oral Sex

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510(K) Number K212928
Device Name Barrier,Std,Oral Sex
Applicant Brazen Goods Inc. dba Lorals
106 1/2 Judge John Aiso St. #305
Los Angeles, CA 90012 US
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Contact Melanie Cristol
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Regulation Number 884.5300

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Classification Product Code MSC
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Date Received 09/14/2021
Decision Date 04/22/2022
Decision SESE - SUBST EQUIV
Classification Advisory Committee OB - Obstetrics/Gynecology
Review Advisory Committee OB - Obstetrics/Gynecology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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