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FDA 510(k)

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM

K-Number: K180663 · 2018-05-18

ApplicantLivermoretech, Inc.
Decision Date2018-05-18
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is a medical device manufactured by Livermoretech, Inc.. It received FDA 510(k) clearance on 2018-05-18 under approval number K180663. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2018-05-18. It is manufactured by Livermoretech, Inc.. The 510(k) number is K180663.

When was LaVid FMTS DIAGNOSTIC X-RAY SYSTEM approved by the FDA?

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM received FDA 510(k) clearance on 2018-05-18, under approval number K180663.

What company makes LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is manufactured by Livermoretech, Inc..

What is the FDA product code for LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

The FDA product code for LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is KPR.

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Related PubMed Literature

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Other Devices by Livermoretech, Inc.

K190935EZER, Portable 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: KPR)

K163203Carestream DRX-EvolutionCarestream Health, Inc. K163115GC70Samsung Electronics Co., Ltd. K152813FS-500DDR Medical Radiographic X-Ray SystemOrich Medical Equipment (Tianjin) Co., Ltd. K162971Multix Fusion MaxSiemens Medical Solutions USA, Inc. K161937CuattroDRCuattro, LLC K162224ArtPix Mobile EZ2GOCmt Medical Technologies, Ltd.

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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