# Stoeckert Instrumente

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 13 (1982–2001): 13 510(k) clearances
- Product codes: DTQ (3), DWB (3), DWF (2), KRI (2), DTW (1), DTR (1), DTB (1)
- Predicates its devices cite: 3 (3 its own); citations of its devices by later devices: 8 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Stockert Instrumente GmbH: 3 (https://510kreport.com/company/stockert-instrumente)
- Sorin Group Deutschland GmbH: 2 (https://510kreport.com/company/sorin-group-deutschland)

## Its most-cited devices
- K950990: Stockert S3 Roller Pump Module Stockert S3 Console (1996), cited by 2
- K982014: Stockert Compact System (1998), cited by 2
- K971520: S3 Cyclic RPM Control (1997), cited by 2
- K955038: Stockert S3 Double Head Pump Module (1996), cited by 1
- K955152: Stockert S3 Ups, LVL CTRL Bubb. Det., Dual Press. CTRL., Temp Mont., Timer (1996), cited by 1

## Recent decisions
- K002273: Stockert A272 Series Pediatric Aortic Cannulae (Jan 29, 2001)
- K001961: Stockert A242 and A252 Series Arterial Femoral Cannulae (Jan 25, 2001)
- K002118: Stockert Compact System Version 2.0 (Aug 9, 2000)
- K992635: Interface Module Iddd (Dec 20, 1999)
- K990512: Stockert Power Supply Unit for S3 Components (Nov 23, 1999)
- K982014: Stockert Compact System (Sep 4, 1998)
- K972321: S3 Mast Pump (Feb 27, 1998)
- K971520: S3 Cyclic RPM Control (Sep 10, 1997)

Source page: https://510kreport.com/company/stoeckert-instrumente