FDA 510(k) Application Details - K190225

Device Classification Name

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510(K) Number K190225
Device Name TAP Blood Collection Device
Applicant Seventh Sense Biosystems, Inc.
200 Boston Avenue, Suite 3700
Medford, MA 02155 US
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Contact Tim Richards
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Regulation Number

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Classification Product Code PRJ
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Date Received 02/05/2019
Decision Date 11/05/2019
Decision SESE - SUBST EQUIV
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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