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FDA 510(k)

CERILLIUM

K-Number: K820049 · 1982-02-22

ApplicantJelrus Technical Products Corp.
Decision Date1982-02-22
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERILLIUM 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 1982-02-22 under 510(k) number K820049. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERILLIUM?

CERILLIUM is a medical device that received FDA 510(k) clearance on 1982-02-22. The listed applicant is Jelrus Technical Products Corp.. The 510(k) number is K820049.

When did CERILLIUM receive FDA 510(k) clearance?

CERILLIUM received FDA 510(k) clearance on 1982-02-22, under 510(k) number K820049.

Who is the listed applicant for CERILLIUM?

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 CERILLIUM?

The FDA product code for CERILLIUM is EJH.

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.

K840254DIAMOND LUSTRE

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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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