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510(k) K133586

VISI MOBILE MONITIORING SYSTEM by Sotera Wireless, Inc. — Product Code MWI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 2013
Date Received
November 21, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type

Other clearances by Sotera Wireless, Inc.

  • K180472 — ViSi Mobile Monitoring System (June 19, 2018)
  • K152341 — ViSi Mobile Monitoring System (December 14, 2015)
  • K142827 — Visi Mobile Monitoring System, Visi Mobile Chest Sensor (July 20, 2015)
  • K150361 — ViSi Mobile Monitoring System (April 30, 2015)
  • K143751 — Visi Mobile Monitoring System (January 23, 2015)
  • K130709 — VISI MOBILE MONITORING SYSTEM (October 7, 2013)
  • K122036 — VISI MOBILE MONITORING SYSTEM (August 15, 2012)
  • K112478 — VISI MOBILE MONITORING SYSTEM (March 22, 2012)

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  • K241958 — WARD-CSS (v1.2.x) (February 14, 2025)
  • K243146 — iCare APP (February 3, 2025)
  • K241411 — Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) (December 20, 2024)
  • K243216 — Sensinel Cardiopulmonary Management (CPM) System (ADCP1100) (December 10, 2024)
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