Home / 510(k) Clearances / K012467

510(k) K012467

SOLAR 8000M SYSTEM by General Electric Medical Systems Information Techn — Product Code DSI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 11, 2002
Date Received
August 1, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Detector And Alarm, Arrhythmia
Device Class
Class II
Regulation Number
870.1025
Review Panel
CV
Submission Type

Other clearances by General Electric Medical Systems Information Techn

  • K023380 — T-WAVE ALTERMANS (TWA) ALGORITHM OPTION (December 3, 2002)
  • K021470 — SEER LIGHT COMPACT DIGITAL HOLTER RECORDER (November 14, 2002)
  • K023100 — ACCUSKETCH CARDIAC QUANTITATIVE SYSTEM W/ ADVANCED ANALYSIS COMPONENTS (October 11, 2002)
  • K021454 — UNITY NETWORK ID (October 1, 2002)
  • K020290 — DASH 3000/4000 PATIENT MONITOR (August 14, 2002)
  • K021366 — MAC-LAB/CARDIOLAB EP/COMBOLAB (July 3, 2002)
  • K020661 — UNITY IS PATIENT VIEWER (May 24, 2002)
  • K021325 — MODIFICATION OF APEXPRO TELEMETRY SYSTEM (May 7, 2002)
  • K020524 — PATIENTNET MONITORING SYSTEM (March 20, 2002)
  • K014108 — MAC 5000 ECG ANALYSIS SYSTEM (January 10, 2002)

Other clearances for product code DSI

  • K243349 — BodyGuardian Remote Monitoring System (BGRMS v3.0) (January 23, 2026)
  • K250356 — MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000) (July 29, 2025)
  • K240177 — Zio AT® device (A100A1001) (October 30, 2024)
  • K230265 — MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection System (October 6, 2023)
  • K231276 — SmartCardia 7L Platform (August 30, 2023)
  • K193104 — Unified Arrhythmia Diagnostic System PocketECG IV (April 9, 2020)
  • K192732 — BodyGuardian Remote Monitoring System (March 26, 2020)
  • K190574 — Patient Assistant Model PA97000 (September 24, 2019)
  • K182532 — Liba3 System (May 15, 2019)
  • K181658 — MobileECG 2 BT (March 26, 2019)