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510(k) K950723

AMBULATORY (HOLTER) RECORDING SYSTEM by Biosensor Corp. — Product Code DQK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1996
Date Received
February 16, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Computer, Diagnostic, Programmable
Device Class
Class II
Regulation Number
870.1425
Review Panel
CV
Submission Type

Other clearances by Biosensor Corp.

  • K990956 — BIOSENSOR HOLTER MONITOR SYSTEM SOFTWARE, MODEL 1005 (June 14, 1999)
  • K974546 — BIOSENSOR HOLTER MONITOR SYSTEM (March 4, 1998)
  • K974192 — BIOSENSOR HOLTER MONITOR SYSTEM (March 4, 1998)
  • K950944 — AMBULATORY (HOLTER) RECORDING SYSTEM (June 18, 1996)
  • K960449 — PC ECG 1200 ECG AND STRESS ELECTROCARDIOGRAPHY TESTING SYSTEM(VERSION 2.90) (May 30, 1996)
  • K943338 — BIOSENSOR BIDOP VASCULAR TEST SYSTEM (April 12, 1996)
  • K922027 — AMBULATORY (HOLTER) RECORDING, MODIFICATION (February 17, 1993)
  • K895266 — AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED (January 26, 1990)
  • K831676 — BIOSENSOR ASC SYSTEM (December 1, 1983)

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