FDA 510(k)

LS OIL

K-Number: K173920 · 2018-10-11

Decision Date2018-10-11

Product CodeEKX

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

LS OIL is a medical device manufactured by J. Morita USA, Inc.. It received FDA 510(k) clearance on 2018-10-11 under approval number K173920. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LS OIL?

LS OIL is a medical device that received FDA 510(k) clearance on 2018-10-11. It is manufactured by J. Morita USA, Inc.. The 510(k) number is K173920.

When was LS OIL approved by the FDA?

LS OIL received FDA 510(k) clearance on 2018-10-11, under approval number K173920.

What company makes LS OIL?

LS OIL is manufactured by J. Morita USA, Inc..

What is the FDA product code for LS OIL?

The FDA product code for LS OIL is EKX.

Other Devices by J. Morita USA, Inc.

K171012Veraview X800 K170275Tri Auto ZX2 K190509Lubrina 2 K2013783D Accuitomo 150N K213477Root ZX3

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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.