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FDA 510(k)

DIAMOND LUSTRE

K-Number: K840254 · 1984-04-25

ApplicantJelrus Technical Products Corp.
Decision Date1984-04-25
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIAMOND LUSTRE is the device name listed in this FDA 510(k) record. The listed applicant is Jelrus Technical Products Corp.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840254. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMOND LUSTRE?

DIAMOND LUSTRE is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Jelrus Technical Products Corp.. The 510(k) number is K840254.

When did DIAMOND LUSTRE receive FDA 510(k) clearance?

DIAMOND LUSTRE received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840254.

Who is the listed applicant for DIAMOND LUSTRE?

The FDA 510(k) record lists Jelrus Technical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAMOND LUSTRE?

The FDA product code for DIAMOND LUSTRE is EJR.

Related Clinical Trials

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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Other records listing Jelrus Technical Products Corp. 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.

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