Rinspiration System, Rinspiration System Short Tip, Models FG01477/FG01703

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

510(k) Number

K041123 ↗

FDA Product Code

DQO

Device Class

Class II

Regulation

21 CFR Part 870.1200

Advisory Committee

Cardiovascular

FDA Decision

SESU

• Rinspiration System

  Class II

  FDA 510(k) K041291 Active Cleared 21 May 2004

• Kerberos Proximal Solutions RISPIRATION System

  Class II

  FDA 510(k) K050130 Active Cleared 13 May 2005

• Kerberos Occluding Guide Catheter and Accessories

  Class II

  FDA 510(k) K041151 Active Cleared 22 Jul 2004

• Rinspiration Catheter System, Models 50135, 550135, P7065, P70135

  Class II

  FDA 510(k) K062275 Active Cleared 20 Sep 2006

• Rinspiration System

  Class II

  FDA 510(k) K031485 Active Cleared 25 Sep 2003