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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 a medical device manufactured by Relievant Medsystems. It received FDA 510(k) clearance on 2017-08-18 under approval 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. It is manufactured by Relievant Medsystems. The 510(k) number is K171143.

When was Relievant Medsystems RF Generator approved by the FDA?

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

What company makes Relievant Medsystems RF Generator?

Relievant Medsystems RF Generator is manufactured by Relievant Medsystems.

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

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

Other Devices by Relievant Medsystems

K153272INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set K170827INTRACEPT Intraosseous Nerve Ablation System K180369Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe) K190504Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator

Related Devices (Code: GXD)

K170242MultiGen™ 2 RF Generator SystemStryker Corporation K181864Polaris RF Ablation SystemBaylis Medical Company, Inc. K201610IonicRF GeneratorABBOTT MEDICAL K192491Coolief Radiofrequency Generator (CRG) SystemAvanos Medical, Inc. K203293Abbott Medical Grounding Pad, model RF-DGP-ISABBOTT MEDICAL K231675OneRF Ablation SystemNeuroone Medical Technologies Corp.

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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