Mercury Medical Disposable Radiofrequency Cannula
FDA 510(k) K000073 · Mercury Medical
510(k) numberK000073
Submission
- Device name
- Mercury Medical Disposable Radiofrequency Cannula
- Applicant
- Mercury Medical
Middleton, MA, US - Received
- January 10, 2000
- Decision date
- March 1, 2000
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code GXI
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|---|---|---|---|
| K253907 | Disposable Radiofrequency CannulaGXI · Traditional | Abbott Medical | 04/16/2026SE |
| K251802 | STAR RF Ablation SystemGXI · Traditional | Merit Medical Systems, Inc. | 02/13/2026SE |
| K251243 | OneRF Trigeminal Nerve Radiofrequency ProbesGXI · Traditional | Neuroone Medical Technologies Corp. | 08/15/2025SE |
| K242841 | Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)GXI · Traditional | Abbott Medical | 05/27/2025SE |
| K250213 | OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN…GXI · Traditional | Stryker Instruments | 05/15/2025SE |
| K241367 | RF CannulaGXI · Traditional | Shanghai Samedical & Plastic Instruments Co., Ltd. | 01/23/2025SE |
| K222281 | Intracept Intraosseous Nerve Ablation SystemGXI · Traditional | Relievant Medsystems, Inc. | 10/26/2022SE |
| K213836 | Intracept Intraosseous Nerve Ablation SystemGXI · Traditional | Relievant Medsystems, Inc. | 03/11/2022SE |
| K203066 | COOLIEF Cooled Radiofrequency Kit AdvancedGXI · Traditional | Avanos Medical, Inc. | 12/22/2020SE |
| K190259 | Vesta RF CannulaGXI · Special | Biomerics | 02/07/2020SE |
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| K083056 | Neo-Stat CO2 <KgCCK · Traditional | 02/23/2009SE |
| K032593 | Mercury Medical Negative Inspiratory Force (Nif) Disposable MonometerBXR · Traditional | 02/03/2004SE |
| K031814 | STATCO2METER, Model 10-55372CCK · Traditional | 08/14/2003SE |
| K031411 | Mini STATCO2 CO2 Detector, Model 10-55371CCK · Traditional | 07/30/2003SE |
| K021576 | Mercury Medical STATCO2 End Tidal CO2 Detector, Model 10-55370CCK · Traditional | 11/04/2002SE |
| K001714 | Mercury Medical Hyperinflation Bag System, Model 83-900-0149NHK · Traditional | 11/03/2000SE |
| K970756 | Mercury Medical Reusable CPR BagBTM · Traditional | 10/31/1997SE |
Questions and answers
When was Mercury Medical Disposable Radiofrequency Cannula cleared by the FDA?
Mercury Medical Disposable Radiofrequency Cannula (K000073) received a 510(k) decision of Substantially Equivalent on March 1, 2000, 51 days after the submission was received.
What is the product code of K000073?
The FDA product code is GXI – Probe, Radiofrequency Lesion, a Class II (moderate risk) device regulated under 21 CFR 882.4725.