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FDA 510(k)

LUXOR PORCELAIN

K-Number: K820057 · 1982-03-02

ApplicantJeneric Ind.
Decision Date1982-03-02
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LUXOR PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1982-03-02 under 510(k) number K820057. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUXOR PORCELAIN?

LUXOR PORCELAIN is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is Jeneric Ind.. The 510(k) number is K820057.

When did LUXOR PORCELAIN receive FDA 510(k) clearance?

LUXOR PORCELAIN received FDA 510(k) clearance on 1982-03-02, under 510(k) number K820057.

Who is the listed applicant for LUXOR PORCELAIN?

The FDA 510(k) record lists Jeneric Ind. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUXOR PORCELAIN?

The FDA product code for LUXOR PORCELAIN is EIH.

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Other records listing Jeneric Ind. as applicant

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Related Devices (Code: EIH)

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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