Case 8000 Exercise Testing System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K991014 ↗

FDA Product Code

LOS

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Solar 7/8000

  Class II

  FDA 510(k) K993757 Active Cleared 23 Mar 2000

• Bis/EEG Module

  Class II

  FDA 510(k) K012466 Active Cleared 1 Oct 2001

• Solar 8000M System Open recall

  Class II

  FDA 510(k) K012467 Active Cleared 11 Feb 2002

• Dash 3000 Patient Monitor Open recall

  Class II

  FDA 510(k) K992929 Active Cleared 26 Nov 1999

• Dash 3000/4000 Patient Monitor Open recall

  Class II

  FDA 510(k) K001359 Active Cleared 18 Jul 2000

• Corometrics Model 171 and 172 Fetal Monitor

  Class II

  FDA 510(k) K991905 Active Cleared 1 Sep 1999

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