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FDA 510(k)

ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400

K-Number: K062716 · 2006-10-27

ApplicantEco-Rx, Inc.
Decision Date2006-10-27
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400 is the device name listed in this FDA 510(k) record. The listed applicant is Eco-Rx, Inc.. It received FDA 510(k) clearance on 2006-10-27 under 510(k) number K062716. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400?

ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400 is a medical device that received FDA 510(k) clearance on 2006-10-27. The listed applicant is Eco-Rx, Inc.. The 510(k) number is K062716.

When did ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400 receive FDA 510(k) clearance?

ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400 received FDA 510(k) clearance on 2006-10-27, under 510(k) number K062716.

Who is the listed applicant for ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400?

The FDA 510(k) record lists Eco-Rx, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400?

The FDA product code for ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400 is FRA.

Related Clinical Trials

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Related Devices (Code: FRA)

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.

K252128Zener® (model ZEN-001-B1)Uvx, Inc.K241140ViroZap Indoor Air Purifier, In Duct Model 1008Applied Photonix, LLCK232642AirKEE T900Healkee Medical Pte, Ltd.K232933AirKEE P900Healkee Medical Pte, Ltd.K232645Airgle Room Air PurifierAirgle CorporationK221540Synexis Sphere RxSynexis, 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.

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