CEREBROVASCULAR DIAGNOSTIC SYSTEM - Cerebrovascular Diagnostic System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K914862 ↗

FDA Product Code

IYN

Models / Variants

Cerebrovascular Diagnostic System

Cds

Device Class

Class II

Regulation

21 CFR Part 892.1550

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Cadence Doppler Ultrasound System

  Class II

  FDA 510(k) K991441 Active Cleared 28 Dec 1999

• Transpect Transcranial Doppler

  Class II

  FDA 510(k) K872292 Active Cleared 14 Aug 1987

• Plethysmograph, Strain Gauge

  Class II

  FDA 510(k) K782132 Active Cleared 26 Feb 1979

• Vasculab #R12B

  Class I

  FDA 510(k) K812608 Active Cleared 2 Oct 1981

• Vasculab Spectrum Analyzer #SP25

  Class II

  FDA 510(k) K820898 Active Cleared 21 Apr 1982

• Vasculab Bi-Directional Doppler, #D10

  Class II

  FDA 510(k) K800768 Active Cleared 8 Jul 1980

See all devices from Medasonics, Inc. →