FDA 510(k) Application Details - K202066

Device Classification Name Computer, Diagnostic, Programmable

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510(K) Number K202066
Device Name Computer, Diagnostic, Programmable
Applicant Abbott Medical
One St. Jude Medical Drive
St. Paul, MN 55117 US
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Contact Alyssa Timmers
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Regulation Number 870.1425

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Classification Product Code DQK
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Date Received 07/27/2020
Decision Date 11/25/2020
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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