Reprieve Endovascular Temperature Therapy System

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K071008 ↗

FDA Product Code

NCX

Device Class

Class II

Regulation

21 CFR Part 870.5900

Advisory Committee

Cardiovascular

FDA Decision

SESU

• Reprieve Endovascular Temperature Therapy System

  Class II

  FDA 510(k) K063405 Active Cleared 8 Jan 2007

• Radiant Medical Endocatheter Temperature Probe

  Class II

  FDA 510(k) K042388 Active Cleared 28 Oct 2004

• Setpoint Endovascular Temperature Management System

  Class II

  FDA 510(k) K012512 Active Cleared 11 Jun 2002

• Setpoint Endovascular Temperature Probe

  Class II

  FDA 510(k) K024327 Active Cleared 25 Mar 2003

• Reprieve Endovascular Temperature Therapy System

  Class II

  FDA 510(k) K071358 Active Cleared 1 Jun 2007