# Kontron Instruments, Inc.

- Location (FDA's records): Everett, MA
- FDA decisions: 58 (1981–1997): 58 510(k) clearances
- Names in FDA's records: Kontron Instruments, Inc. (57); Kontron Instruments , Ltd. (1)
- Product codes: DSP (17), DRT (5), DPS (5), DQA (3), DXN (2), IYO (2), HGL (2), HGM (2), DSI (2), CBK (1), DQK (1), DXG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 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
- Arrow Intl., Inc.: 3 (https://510kreport.com/company/arrow-intl)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Linde Medical Sensors AG: 1 (https://510kreport.com/company/linde-medical-sensors)
- Datascope Corp.: 1 (https://510kreport.com/company/datascope)

## Its most-cited devices
- K892799: 8 FR Percutan Double Lumen Intra-Aortic Balloon (1989), cited by 2
- K905313: Kontron Intra-Aortic Balloon Pump, Model Kaat II (1991), cited by 2
- K890299: Kontron Pulse Oximeter 7840 (1989), cited by 1
- K892222: 9.5F Percu Double Lumen Intra-Aortic Balloon (1990), cited by 1

## Recent decisions
- K971038: Kontron Kolormon Plus Ecg with Respiration Module (Sep 24, 1997)
- K932268: Modifications to Intra-Aortic Balloons (Dec 15, 1993)
- K925248: Modification of Intra-Aortic Balloon Catheters (Sep 27, 1993)
- K923603: Intra-Aortic Balloon Pump Catheter - Modification (Mar 8, 1993)
- K905313: Kontron Intra-Aortic Balloon Pump, Model Kaat II (Jun 19, 1991)
- K903344: 9.5 FR Percutaneous DB Lumen 40CC Flexi-Cath (TM) (Jan 15, 1991)
- K896437: Kontron Sigma 44 HVCD Ultrasound Imaging System (Dec 3, 1990)
- K892222: 9.5F Percu Double Lumen Intra-Aortic Balloon (Sep 14, 1990)

Source page: https://510kreport.com/company/kontron-instruments