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FDA 510(k)

EZER, Portable X-ray System

K-Number: K190935 · 2019-12-19

ApplicantLivermoretech, Inc.
Decision Date2019-12-19
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EZER, Portable X-ray System is a medical device manufactured by Livermoretech, Inc.. It received FDA 510(k) clearance on 2019-12-19 under approval number K190935. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZER, Portable X-ray System?

EZER, Portable X-ray System is a medical device that received FDA 510(k) clearance on 2019-12-19. It is manufactured by Livermoretech, Inc.. The 510(k) number is K190935.

When was EZER, Portable X-ray System approved by the FDA?

EZER, Portable X-ray System received FDA 510(k) clearance on 2019-12-19, under approval number K190935.

What company makes EZER, Portable X-ray System?

EZER, Portable X-ray System is manufactured by Livermoretech, Inc..

What is the FDA product code for EZER, Portable X-ray System?

The FDA product code for EZER, Portable X-ray System is EHD.

Related Clinical Trials

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Other Devices by Livermoretech, Inc.

K180663LaVid FMTS DIAGNOSTIC X-RAY SYSTEM K193535EZER, Portable X-ray System K200022FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System K193644E-COM DR-2000 DR K244049Europa (Alternative: AiRTouch) portable X-ray system

Related Devices (Code: EHD)

K161063EzRay Air (Model VEX-P300)VATECH Co., Ltd. K160458BI IMAGE-X EVOLUTIONRadiotecnologia Industrial S.A. DE C.V. K173319KaVo NOMAD Pro 2 Handheld X-ray SystemAribex K170967Intraskan DC PlusSkanray Technologies Private Limited K163705EzRay Air WVATECH Co., Ltd. K163519RX DCCefla S.C.

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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