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510(k) K943338

BIOSENSOR BIDOP VASCULAR TEST SYSTEM by Biosensor Corp. — Product Code JAF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 1996
Date Received
July 12, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Ultrasonic, Nonfetal
Device Class
Class II
Regulation Number
892.1540
Review Panel
RA
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)
  • K950723 — AMBULATORY (HOLTER) RECORDING SYSTEM (February 9, 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)

Other clearances for product code JAF

  • K242487 — Laminar P1 (LDH-HW-001) (December 13, 2024)
  • K141657 — THD REVOLUTION (February 24, 2015)
  • K110628 — SIMPLEABI (May 12, 2011)
  • K093393 — LIFEDOP MODEL 300ABI (December 24, 2009)
  • K090009 — THD SLIDE ONE (January 28, 2009)
  • K081429 — THD SLIDE (July 30, 2008)
  • K070815 — THD (June 20, 2007)
  • K063600 — VISTA AVS (December 19, 2006)
  • K060064 — STETHOFLUX (April 10, 2006)
  • K052067 — DOPPLER GUIDED PROCTOSCOPE, MODEL 500H (August 29, 2005)