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FDA 510(k)

Relievant Medsystems RF Generator

K-Number: K171143 · 2017-08-18

ApplicantRelievant Medsystems
Decision Date2017-08-18
Product CodeGXD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Relievant Medsystems RF Generator is the device name listed in this FDA 510(k) record. The listed applicant is Relievant Medsystems. It received FDA 510(k) clearance on 2017-08-18 under 510(k) number K171143. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Relievant Medsystems RF Generator?

Relievant Medsystems RF Generator is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is Relievant Medsystems. The 510(k) number is K171143.

When did Relievant Medsystems RF Generator receive FDA 510(k) clearance?

Relievant Medsystems RF Generator received FDA 510(k) clearance on 2017-08-18, under 510(k) number K171143.

Who is the listed applicant for Relievant Medsystems RF Generator?

The FDA 510(k) record lists Relievant Medsystems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Relievant Medsystems RF Generator?

The FDA product code for Relievant Medsystems RF Generator is GXD.

Other records listing Relievant Medsystems as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222281Intracept Intraosseous Nerve Ablation SystemK213836Intracept Intraosseous Nerve Ablation SystemK190504Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF GeneratorK180369Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)K170827INTRACEPT Intraosseous Nerve Ablation SystemK153272INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set

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Related Devices (Code: GXD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251247GX1 Radiofrequency Generator Kit (RFG-X1-120V); GX1 Radiofrequency Generator Kit (RFG-X1-220V); GX1 Radiofrequency Generator Kit (RFG-X1-240V); GX1 System Release Rest of World (GX1-SYS-ROW); GX1 Radiofrequency Generator (51779845-01); GX1 Radiofrequency Generator (51779845-02); GX1 Radiofrequency Generator (51779845-03)Boston Scientific Neuromodulation CorporationK242057COOLIEF* Radiofrequency Generator (CRG-BASIC, CRG-BASIC-R, CRG-ADVANCED, CRG-ADVANCED-R)Avanos Medical, Inc.K232632Racz Neurostat RF GeneratorEpimed InternationalK231675OneRF Ablation SystemNeuroone Medical Technologies Corp.K220122APEX 6Rf Innovations, Inc.K203293Abbott Medical Grounding Pad, model RF-DGP-ISABBOTT MEDICAL

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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