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 the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2018-10-11 under 510(k) 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. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K173920.

When did LS OIL receive FDA 510(k) clearance?

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

Who is the listed applicant for LS OIL?

The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LS OIL?

The FDA product code for LS OIL is EKX.

Other records listing J. Morita USA, Inc. as applicant

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.

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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.