Home › Device types › IKD
Cable, Electrode
FDA product code IKD · Class 2 · Physical Medicine
6,398
Registered devices
459
Adverse events
11
Recalls
6
510(k) clearances
Devices with this code
Kendall — Cardinal Health, Inc.Surelead — Authentic MedicalEnSite™ — ST. JUDE MEDICAL, INC.Kendall — Cardinal Health 200, LLCCadwell Extension Lead Wire — CADWELL INDUSTRIES, INC.C.M.P. Cable — C.M.P. Canadian Medical Products IncAirRay® Electrode Connection Cable US — CorTec GmbHAPK — APK Technology Co.,Ltd.TECH-ATTACH Connection System Cable — Ad-Tech Medical Instrument CorporationOrantech — Orantech Inc.Seer Home — SEER MEDICAL HOLDINGS LIMITEDAPK — APK Technology Co.,Ltd.FMT — METKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETIKendall — Cardinal Health, Inc.N/A — PMT CORPORATIONC.M.P. Cable — C.M.P. Canadian Medical Products IncNAMIC — NAVILYST MEDICAL, INC.Norav Medical — Norav Medical GmbHN/A — INNOVATIVE HEALTH LLCKendall — Cardinal Health, Inc.Orantech — Orantech Inc.APK — APK Technology Co.,Ltd.Alpine Biomed — Alpine Biomed ApSAPK — APK Technology Co.,Ltd.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-07-02 | Stryker Sustainability Solutions | Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, dif |
| 2021-08-09 | Ad-Tech Medical Instrument Corporation | Incorrect version of labels were used. |
| 2021-08-09 | Ad-Tech Medical Instrument Corporation | Incorrect version of labels were used. |
| 2021-08-09 | Ad-Tech Medical Instrument Corporation | Incorrect version of labels were used. |
| 2019-02-22 | GE Healthcare, LLC | The Integrated ECG cable with 3-lead leadwires can short circuit during defibrillation and conduct 25% of the defibrillation energy away from the patient. |
| 2017-03-31 | Oscor, Inc. | The Reusable Oscor ATAR extension cables could separate from the connector during use. |
| 2017-03-31 | Oscor, Inc. | The Reusable Oscor ATAR extension cables could separate from the connector during use. |
| 2016-03-29 | Ad-Tech Medical Instrument Corporation | Ad-Tech is recalling unopened/unused sterile cables intended to be used only with all compatible Ad-Tech electrodes for the purpose of connecting these electrod |
| 2011-06-01 | St. Jude Medical | St. Jude Medical is recalling a single lot (3334664) of Supreme Electrophysiology Extension Cable which were packaged with a Quadripolar cable instead of a hexa |
| 2011-02-08 | Vermed, Inc. | Vermed kits contain a product component (Triad Alcohol Prep Pads) recalled due to potential Bacillus cereus contamination. |
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