Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RIA Safeguard

K-Number: K222416 · 2023-05-01

ApplicantRia Tech Co., Ltd.
Decision Date2023-05-01
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RIA Safeguard is a medical device manufactured by Ria Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-01 under approval 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. It is manufactured by Ria Tech Co., Ltd.. The 510(k) number is K222416.

When was RIA Safeguard approved by the FDA?

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

What company makes RIA Safeguard?

RIA Safeguard is manufactured by Ria Tech Co., Ltd..

What is the FDA product code for RIA Safeguard?

The FDA product code for RIA Safeguard is FRF.

Related Devices (Code: FRF)

K200321Novaerus NV1050Novaerus Us, Inc. K211507Airdog X5 Recirculating Air Cleaner (model KJ300F-X5)Beiang Air Tech , Ltd. K220990Qorda QD1Winix, Inc. K220298CerroZone MobileCerrozone K223835MA-40, MA-112Medify Air, LLC K242102CerroZone MiniCerrozone, LLC

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.

↑