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510(k) K837481

BF24 DOPPLER MODEL P872 AND P874 by Medasonics, Inc.

K837481 is an FDA 510(k) premarket notification submitted by Medasonics, Inc. for the device "BF24 DOPPLER MODEL P872 AND P874". The FDA issued a decision of Substantially Equivalent on June 24, 1983. Medasonics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 24, 1983
Date Received
May 9, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Medasonics, Inc.

  • K991441 — CADENCE DOPPLER ULTRASOUND SYSTEM (December 28, 1999)
  • K962796 — NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEM (January 21, 1997)
  • K961116 — FIRST BEAT/CARDIO BEAT/CALC (August 8, 1996)
  • K914862 — CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDS (December 3, 1992)
  • K911453 — OBTRASOUND STETHOSCOPE FETAL CALC (June 20, 1991)
  • K882018 — MEDACORD PVL, PERSONAL VASCULAR LABORATORY (September 21, 1988)
  • K872292 — TRANSPECT TRANSCRANIAL DOPPLER (August 14, 1987)
  • K854734 — MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLE (February 10, 1986)
  • K833588 — VASCULAR LABORATORY TREADMILL VT1 (November 14, 1983)
  • K831393 — VASCULAB BLOOD PRESSURE CUFF (June 16, 1983)

FDA data resources