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510(k) K202138

Cardiac Trigger Monitor by Ivy Biomedical Systems, Inc. — Product Code DRT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 2021
Date Received
July 31, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type

Other clearances by Ivy Biomedical Systems, Inc.

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  • K171778 — MR Wireless Gating System, Model WGS-100 (March 14, 2018)
  • K170828 — Cardiac Trigger Monitor (May 17, 2017)
  • K151781 — Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor (May 27, 2016)
  • K110987 — CARDIAC TRIGGER MONITOR (July 22, 2011)
  • K091787 — MODEL 6000 TWO PARAMETER BEDSIDE MONITOR (October 9, 2009)
  • K091985 — UNIVERSAL PHYSIOLOGICAL MEASUREMENT MODULE (July 24, 2009)
  • K083854 — CARDIAC TRIGGER, MODEL: CTM300 (February 13, 2009)

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