FDA 510(k) Application Details - K151275

Device Classification Name Hysteroscope (And Accessories)

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510(K) Number K151275
Device Name Hysteroscope (And Accessories)
Applicant nVision Medical
250 King Street, #676
San Francisco, CA 94107 US
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Contact Surbhi Sarna
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Regulation Number 884.1690

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Classification Product Code HIH
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Date Received 05/13/2015
Decision Date 11/13/2015
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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