Stockert S3 Ups, Lvl Ctrl Bubb. Det., Dual Press. Ctrl., Temp Mont., Timer

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

510(k) Number

K955152 ↗

FDA Product Code

DTW

Device Class

Class II

Regulation

21 CFR Part 870.4340

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Stockert Compact System Version 2.0

  Class II

  FDA 510(k) K002118 Active Cleared 9 Aug 2000

• Interface Module Iddd

  Class I

  FDA 510(k) K992635 Active Cleared 20 Dec 1999

• Stockert S3 Double Head Pump Module

  Class II

  FDA 510(k) K955038 Active Cleared 21 Feb 1996

• S3 Cyclic Rpm Control

  Class II

  FDA 510(k) K971520 Active Cleared 10 Sep 1997

• Stockert A272 Series Pediatric Aortic Cannulae

  Class II

  FDA 510(k) K002273 Active Cleared 29 Jan 2001

• Stockert Compact System

  Class II

  FDA 510(k) K982014 Active Cleared 4 Sep 1998

See all devices from Stoeckert Instrumente →