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FDA 510(k)

LITE MINERAL OIL

K-Number: K022332 · 2002-08-23

Applicant<Genx> Intl., Inc.
Decision Date2002-08-23
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LITE MINERAL OIL is the device name listed in this FDA 510(k) record. The listed applicant is <Genx> Intl., Inc.. It received FDA 510(k) clearance on 2002-08-23 under 510(k) number K022332. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITE MINERAL OIL?

LITE MINERAL OIL is a medical device that received FDA 510(k) clearance on 2002-08-23. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K022332.

When did LITE MINERAL OIL receive FDA 510(k) clearance?

LITE MINERAL OIL received FDA 510(k) clearance on 2002-08-23, under 510(k) number K022332.

Who is the listed applicant for LITE MINERAL OIL?

The FDA 510(k) record lists <Genx> Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITE MINERAL OIL?

The FDA product code for LITE MINERAL OIL is MQL.

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Related Devices (Code: MQL)

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

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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