# Cordis Corp., A Johnson & Johnson Co.

- Location (FDA's records): Fremont, CA
- FDA decisions: 11 (1999–2015): 11 510(k) clearances
- Names in FDA's records: Cordis Corp., A Johnson & Johnson Co. (5); Cordis, A Johnson & Johnson Co. (4); Cordis Corporation, A Johnson & Johnson Co. (1); Cordis Corporation, A Johnson & Johnson Company (1)
- Product codes: PDU (4), DTK (2), FGE (2), DQY (2), NTE (1)
- Predicates its devices cite: 17 (3 its own); citations of its devices by later devices: 17 (3 its own)
- Recalls linked to its devices: 3 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cordis Corp.: 11 (https://510kreport.com/company/cordis)
- Lumend, Inc.: 1 (https://510kreport.com/company/lumend)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Firms that cite its devices most
- Cordis Corp.: 7 (https://510kreport.com/company/cordis)
- Angioscore, Inc.: 3 (https://510kreport.com/company/angioscore)
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- LimFlow, Inc.: 1 (https://510kreport.com/company/limflow)
- Cordis Europa, N.V.: 1 (https://510kreport.com/company/cordis-europa)

## Its most-cited devices
- K992755: Cordis Palmaz Corinthian Transhepatic Biliary Stent and Delivery System, Cordis Crimping Tools, Cordis Introducer Tube (1999), cited by 4
- K013581: Cordis Aviator Peripheral Dilatation Catheter (2001), cited by 4
- K083814: Outback LTD RE-Entry Catheter, Model: OTB42120 (2009), cited by 2
- K062531: Angioguard XP Emboli Capture Guidewire and Angioguard RX Emboli Capture Guidewire (2006), cited by 2
- K012090: Cordis Palmaz Genesis Transhepatic Biliary Stent (2001), cited by 2
- K150836: OUTBACK Elite Re-Entry Catheter (2015), cited by 1

## Recent decisions
- K150187: ELITECROSS Support Catheter (May 19, 2015)
- K150836: OUTBACK Elite Re-Entry Catheter (Apr 29, 2015)
- K140438: Micro Guide Catheter Elite (Nov 14, 2014)
- K140286: Optease Vena Cava Filter and Optease Retrieval Cathteter (Mar 7, 2014)
- K131225: Adroit Guiding Catheter (May 29, 2013)
- K091077: Optease Vena Cava Filter and Retrieval Catheter (Feb 4, 2010)
- K083814: Outback LTD RE-Entry Catheter, Model: OTB42120 (Jan 13, 2009)
- K062531: Angioguard XP Emboli Capture Guidewire and Angioguard RX Emboli Capture Guidewire (Sep 22, 2006)

Source page: https://510kreport.com/company/cordis-a-johnson-johnson