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510(k) K182981

Confirm Rx Insertable Cardiac Monitor by Abbott — Product Code MXC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 2019
Date Received
October 29, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)
Device Class
Class II
Regulation Number
870.2800
Review Panel
CV
Submission Type

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Other clearances for product code MXC

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  • K202876 — Confirm Rx Insertable Cardiac Monitor (December 1, 2020)
  • K202888 — Confirm Rx Insertable Cardiac Monitor (November 23, 2020)
  • K193310 — myMerlin Mobile Application (Android), myMerlin Mobile Application (iOS) (March 17, 2020)
  • K192593 — Confirm Rx Insertable Cardiac Monitor (October 18, 2019)
  • K190295 — Confirm Rx Insertable Cardiac Monitor (April 10, 2019)
  • K173232 — myMerlin(TM) Mobile Application Model APP1001 (November 2, 2017)
  • K163407 — Confirm Rx Insertable Cardiac Monitor (ICM) System (September 29, 2017)
  • K133481 — SJM CONFIRM IMPLANTABLE CARDIAC MONITOR (ICM) (May 28, 2014)