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FDA 510(k)

RF-Relief

K-Number: K181095 · 2018-07-24

Decision Date2018-07-24
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RF-Relief is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2018-07-24 under 510(k) number K181095. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF-Relief?

RF-Relief is a medical device that received FDA 510(k) clearance on 2018-07-24. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K181095.

When did RF-Relief receive FDA 510(k) clearance?

RF-Relief received FDA 510(k) clearance on 2018-07-24, under 510(k) number K181095.

Who is the listed applicant for RF-Relief?

The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RF-Relief?

The FDA product code for RF-Relief is PBX.

Other records listing El Global Trade, Ltd. 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.

View all 10 devices →

Related Devices (Code: PBX)

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.

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.