FDA 510(k) Application Details - K190932

Device Classification Name Marker, Radiographic, Implantable

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510(K) Number K190932
Device Name Marker, Radiographic, Implantable
Applicant Health Beacons, Inc.
34 Walden St. #753
Concord, MA 01742 US
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Contact Nancy Confrey
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Regulation Number 878.4300

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Classification Product Code NEU
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Date Received 04/10/2019
Decision Date 09/13/2019
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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