FDA 510(k)

RIA Safeguard

K-Number: K222416 · 2023-05-01

Decision Date2023-05-01

Product CodeFRF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

RIA Safeguard is the device name listed in this FDA 510(k) record. The listed applicant is Ria Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-01 under 510(k) number K222416. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA Safeguard?

RIA Safeguard is a medical device that received FDA 510(k) clearance on 2023-05-01. The listed applicant is Ria Tech Co., Ltd.. The 510(k) number is K222416.

When did RIA Safeguard receive FDA 510(k) clearance?

RIA Safeguard received FDA 510(k) clearance on 2023-05-01, under 510(k) number K222416.

Who is the listed applicant for RIA Safeguard?

The FDA 510(k) record lists Ria Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA Safeguard?

The FDA product code for RIA Safeguard is FRF.

Related Devices (Code: FRF)

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.

K251872Biomoneta Avata RxBiomoneta Research Private Limited K242102CerroZone MiniCerrozone, LLC K240696Airdog X8 Air Purifier (KJ800F-X8)Suzhou Beiang Smart Technology Co., Ltd.K223835MA-40, MA-112Medify Air, LLC K211507Airdog X5 Recirculating Air Cleaner (model KJ300F-X5)Beiang Air Tech , Ltd.K220990Qorda QD1Winix, Inc.

Official Source

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