Tri-Loop Microwave Ablation Probe
FDA 510(k) K032047 · Vivant Medical, Inc.
510(k) numberK032047
Submission
- Device name
- Tri-Loop Microwave Ablation Probe
- Applicant
- Vivant Medical, Inc.
Mountain View, CA, US - Received
- July 2, 2003
- Decision date
- August 6, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GEI – Electrosurgical, Cutting & Coagulation & Accessories
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Specialty
- General, Plastic Surgery
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Other 510(k)s with product code GEI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254185 | Potenza PrimeGEI · Traditional | Jeisys Medical Incorporated | 09/11/2026SE |
| K262364 | Ellian Enigma RF DeviceGEI · Traditional | Ellian Corp | 09/02/2026SE |
| K253859 | Scarlet Pro (Scarlet Pro)GEI · Traditional | VIOL Co., Ltd. | 08/27/2026SE |
| K252535 | Inno-Switch Laparoscopic InstrumentsGEI · Traditional | Taiwan Surgical Corporation | 08/25/2026SE |
| K261179 | AlphaTriPart - Monopolar MIC InstrumentsGEI · Traditional | Gimmi GmbH | 07/22/2026SE |
| K253504 | VolnewmerGEI · Traditional | Classys, Inc. | 07/13/2026SE |
| K254056 | THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35…GEI · Traditional | Olympus Medical Systems Corp. | 07/01/2026SE |
| K253484 | Lutronic GeniusGEI · Traditional | Cynosure Lutronic Technology Corporation | 06/29/2026SE |
| K251492 | Irrigation Tubing Bipolar Cord SetGEI · Traditional | New Deantronics Taiwan , Ltd. | 06/29/2026SE |
| K260636 | Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingGEI · Traditional | Stryker Sustainability Solutions | 06/18/2026SE |
More from Stryker Sustainability Solutions
| 510(k) | Device | Decision |
|---|---|---|
| K050223 | Vivawave Microwave Ablation System, Coaxial IntroducerGEI · Special | 02/24/2005SE |
| K040279 | Vivaring Microwave Ablation ProbeGEI · Special | 03/02/2004SE |
| K032702 | Vivatip Microwave Ablation ProbeGEI · Special | 10/03/2003SE |
| K031556 | Vivatherm Themperature Measurement SystemFLL · Traditional | 06/23/2003SE |
| K023311 | Loop Microwave Ablation ProbeGEI · Traditional | 04/09/2003SE |
| K022286 | Encircle Localization DeviceKNW · Traditional | 10/11/2002SE |
| K011676 | Vivawave Microwave SystemNEY · Traditional | 06/18/2002SE |
| K003439 | Vivant Breast Lesion Localization DeviceKNW · Traditional | 12/15/2000SE |
| K000278 | Vivant Medical Biopsy Marker SystemFZP · Traditional | 06/23/2000SE |
Questions and answers
When was Tri-Loop Microwave Ablation Probe cleared by the FDA?
Tri-Loop Microwave Ablation Probe (K032047) received a 510(k) decision of Substantially Equivalent on August 6, 2003, 35 days after the submission was received.
What is the product code of K032047?
The FDA product code is GEI – Electrosurgical, Cutting & Coagulation & Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4400.